A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15271876



Internal ID5273692
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636755
Supporting Variants
SamplesNA18519
Known GenesIGDCC3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15271876
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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