A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3726744



Internal ID18678339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:9626042..9668155hg38UCSC Ensembl
Innerchr2:9766171..9808284hg19UCSC Ensembl
Innerchr2:9683622..9725735hg18UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3842114
hg1942114
hg1842114
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1011802
Supporting Variants
Samples
Known GenesYWHAQ
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3726744
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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