A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042120



Internal ID19131339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:71182215..71250508hg38UCSC Ensembl
Innerchr13:71756347..71824640hg19UCSC Ensembl
Innerchr13:70654348..70722641hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3868294
hg1968294
hg1868294
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3530498
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)nsv1042120
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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