A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3729351



Internal ID19027632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:212351707..212425799hg38UCSC Ensembl
Innerchr2:213216431..213290523hg19UCSC Ensembl
Innerchr2:212924676..212998768hg18UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg3874093
hg1974093
hg1874093
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003694
Supporting Variants
Samples
Known GenesERBB4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3729351
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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