A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694737



Internal ID15084703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:231515645..231568983hg38UCSC Ensembl
Innerchr1:231651391..231704729hg19UCSC Ensembl
Innerchr1:229718014..229771352hg18UCSC Ensembl
Innerchr1:227958126..228011464hg17UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg3853339
hg1953339
hg1853339
hg1753339
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516935
Supporting Variants
Samples
Known GenesTSNAX, TSNAX-DISC1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694737
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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