A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997931



Internal ID19157467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:147753334..147819320hg38UCSC Ensembl
Innerchr3:147471121..147537107hg19UCSC Ensembl
Innerchr3:148953811..149019797hg18UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3865987
hg1965987
hg1865987
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3606168
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)nsv997931
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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