A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636844



Internal ID7023638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:70735243..70761071hg38UCSC Ensembl
Innerchr15:70735743..70760571hg38UCSC Ensembl
Outerchr15:70734243..70762071hg38UCSC Ensembl
chr15:71027582..71053410hg19UCSC Ensembl
Innerchr15:71028082..71052910hg19UCSC Ensembl
Outerchr15:71026582..71054410hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3825829
hg1925829
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15284111
SamplesNA18572
Known GenesUACA
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636844
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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