A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701396



Internal ID15091362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:226149346..226157320hg38UCSC Ensembl
Innerchr2:227014062..227022036hg19UCSC Ensembl
Innerchr2:226722306..226730280hg18UCSC Ensembl
Innerchr2:226839567..226847541hg17UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg387975
hg197975
hg187975
hg177975
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525291
Supporting Variants
Samples
Known GenesLOC646736
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701396
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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