A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3585621



Internal ID18883902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:211487947..211551490hg38UCSC Ensembl
Innerchr2:212352672..212416215hg19UCSC Ensembl
Innerchr2:212060917..212124460hg18UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg3863544
hg1963544
hg1863544
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1013164
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)nssv3585621
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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