A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3577108



Internal ID18875389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:14868741..14924450hg38UCSC Ensembl
Innerchr2:15008865..15064574hg19UCSC Ensembl
Innerchr2:14926316..14982025hg18UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3855710
hg1955710
hg1855710
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1000487
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)nssv3577108
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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