A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636755



Internal ID6676862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65345168..65346228hg38UCSC Ensembl
Innerchr15:65345186..65346210hg38UCSC Ensembl
Outerchr15:65345150..65346246hg38UCSC Ensembl
chr15:65637506..65638566hg19UCSC Ensembl
Innerchr15:65637524..65638548hg19UCSC Ensembl
Outerchr15:65637488..65638584hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg381061
hg191061
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15271876, essv15271874, essv15271875
SamplesHG03190, NA18519, HG02010
Known GenesIGDCC3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636755
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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