A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3585672



Internal ID18883953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:212505966..212548507hg38UCSC Ensembl
Innerchr2:213370690..213413231hg19UCSC Ensembl
Innerchr2:213078935..213121476hg18UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg3842542
hg1942542
hg1842542
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1014479
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)nssv3585672
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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