A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705436



Internal ID15442088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:184319686..184321381hg38UCSC Ensembl
Innerchr1:184288820..184290515hg19UCSC Ensembl
Innerchr1:182555443..182557138hg18UCSC Ensembl
Innerchr1:181020477..181022172hg17UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg381696
hg191696
hg181696
hg171696
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528772
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705436
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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