A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3577107



Internal ID18528702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:14773854..14881021hg38UCSC Ensembl
Innerchr2:14913978..15021145hg19UCSC Ensembl
Innerchr2:14831429..14938596hg18UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38107168
hg19107168
hg18107168
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1009799
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3577107
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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