A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636256



Internal ID7023052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42096891..42100177hg38UCSC Ensembl
Innerchr15:42096891..42100177hg38UCSC Ensembl
Outerchr15:42096628..42100436hg38UCSC Ensembl
chr15:42389089..42392375hg19UCSC Ensembl
Innerchr15:42389089..42392375hg19UCSC Ensembl
Outerchr15:42388826..42392634hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg383287
hg193287
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15230753, essv15230744, essv15230746, essv15230745, essv15230751, essv15230739, essv15230749, essv15230740, essv15230750, essv15230752, essv15230748, essv15230741, essv15230747, essv15230743, essv15230742
SamplesHG02574, HG03057, HG02012, HG03069, HG03478, HG02541, NA20291, NA19130, HG02427, HG03054, HG03547, HG03457, HG03049, NA19116, NA19312
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636256
Frequency
Sample Size2504
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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