A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701050



Internal ID15091016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:6696374..6701201hg38UCSC Ensembl
Innerchr1:6756434..6761261hg19UCSC Ensembl
Innerchr1:6679021..6683848hg18UCSC Ensembl
Innerchr1:6690700..6695527hg17UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg384828
hg194828
hg184828
hg174828
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525013
Supporting Variants
Samples
Known GenesDNAJC11
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701050
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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