A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619794



Internal ID7006668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15797314..15810798hg38UCSC Ensembl
Innerchr9:15797314..15810798hg38UCSC Ensembl
Outerchr9:15796814..15811298hg38UCSC Ensembl
chr9:15797312..15810796hg19UCSC Ensembl
Innerchr9:15797312..15810796hg19UCSC Ensembl
Outerchr9:15796812..15811296hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3813485
hg1913485
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13408162
SamplesHG03446
Known GenesCCDC171
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619794
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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