A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv692602



Internal ID15429254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:94666373..94687706hg38UCSC Ensembl
Innerchr1:95131929..95153262hg19UCSC Ensembl
Innerchr1:94904517..94925850hg18UCSC Ensembl
Innerchr1:94843950..94865283hg17UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3821334
hg1921334
hg1821334
hg1721334
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517330
Supporting Variants
Samples
Known GenesLINC01057
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv692602
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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