A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041977



Internal ID19131196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:38388128..38428787hg38UCSC Ensembl
Innerchr13:38962265..39002924hg19UCSC Ensembl
Innerchr13:37860265..37900924hg18UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3840660
hg1940660
hg1840660
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3523379
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)nsv1041977
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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