A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv693621



Internal ID15083587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:231515645..231677388hg38UCSC Ensembl
Innerchr1:231651391..231813134hg19UCSC Ensembl
Innerchr1:229718014..229879757hg18UCSC Ensembl
Innerchr1:227958126..228119869hg17UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg38161744
hg19161744
hg18161744
hg17161744
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516935
Supporting Variants
Samples
Known GenesDISC1, LINC00582, TSNAX, TSNAX-DISC1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv693621
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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