A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3729341



Internal ID19027622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:212251896..212314015hg38UCSC Ensembl
Innerchr2:213116621..213178740hg19UCSC Ensembl
Innerchr2:212824866..212886985hg18UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg3862120
hg1962120
hg1862120
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1011111
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)nssv3729341
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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