A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637180



Internal ID7023974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89005704..89008312hg38UCSC Ensembl
Innerchr15:89005714..89008302hg38UCSC Ensembl
Outerchr15:89005694..89008322hg38UCSC Ensembl
chr15:89548935..89551543hg19UCSC Ensembl
Innerchr15:89548945..89551533hg19UCSC Ensembl
Outerchr15:89548925..89551553hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg382609
hg192609
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15317050, essv15317031, essv15317047, essv15317049, essv15317046, essv15317041, essv15317042, essv15317052, essv15317034, essv15317053, essv15317030, essv15317036, essv15317043, essv15317055, essv15317044, essv15317045, essv15317035, essv15317054, essv15317039, essv15317040, essv15317028, essv15317033, essv15317037, essv15317029, essv15317026, essv15317051, essv15317032, essv15317048, essv15317038, essv15317027
SamplesHG02890, HG02610, HG03175, NA19819, HG02589, HG03099, NA19119, HG01110, NA19130, HG01398, HG02623, HG02819, NA18933, NA18516, HG01142, HG02307, HG02757, HG02585, HG02667, NA18909, HG03433, HG02839, HG03157, HG03063, HG02768, HG02676, HG02763, HG02629, HG03129, HG03271
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637180
Frequency
Sample Size2504
Observed Gain0
Observed Loss30
Observed Complex0
Frequencyn/a


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