A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv660368



Internal ID15050334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:61972200..61976116hg38UCSC Ensembl
Innerchr1:62437872..62441788hg19UCSC Ensembl
Innerchr1:62210460..62214376hg18UCSC Ensembl
Innerchr1:62149893..62153809hg17UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg383917
hg193917
hg183917
hg173917
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517696
Supporting Variants
Samples
Known GenesINADL
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv660368
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