A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698582



Internal ID15088548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:101704739..102410836hg38UCSC Ensembl
Innerchr1:102170295..102876392hg19UCSC Ensembl
Innerchr1:101942883..102648980hg18UCSC Ensembl
Innerchr1:101882316..102588413hg17UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38706098
hg19706098
hg18706098
hg17706098
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522921
Supporting Variants
Samples
Known GenesDNAJA1P5, MIR548AI, OLFM3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698582
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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