A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9760444



Internal ID18734690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:32160325..32160572hg38UCSC Ensembl
Outerchr3:32160250..32160625hg38UCSC Ensembl
Innerchr3:32201817..32202064hg19UCSC Ensembl
Outerchr3:32201742..32202117hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38376
hg19376
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3561697
Supporting Variants
Samples
Known GenesGPD1L
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9760444
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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