A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997659



Internal ID19157196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:112380301..112416840hg38UCSC Ensembl
Innerchr3:112099148..112135687hg19UCSC Ensembl
Innerchr3:113581838..113618377hg18UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg3836540
hg1936540
hg1836540
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3604421
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)nsv997659
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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