A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3726655



Internal ID19024936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:711922..948729hg38UCSC Ensembl
Innerchr2:711922..944415hg19UCSC Ensembl
Innerchr2:701922..934415hg18UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg38236808
hg19232494
hg18232494
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1010340
Supporting Variants
Samples
Known GenesLINC01115
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3726655
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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