A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997333



Internal ID19156871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:34692520..34754096hg38UCSC Ensembl
Innerchr3:34734012..34795588hg19UCSC Ensembl
Innerchr3:34709016..34770592hg18UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3861577
hg1961577
hg1861577
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4715n100
Supporting Variantsnssv3589593, nssv3589592
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)nsv997333
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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