A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv689111



Internal ID15425763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:56262574..56266008hg38UCSC Ensembl
Innerchr1:56728246..56731680hg19UCSC Ensembl
Innerchr1:56500834..56504268hg18UCSC Ensembl
Innerchr1:56440267..56443701hg17UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg383435
hg193435
hg183435
hg173435
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516750
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv689111
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer