A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039781



Internal ID18782312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:96536143..96787023hg38UCSC Ensembl
Innerchr13:97188397..97439277hg19UCSC Ensembl
Innerchr13:95986398..96237278hg18UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38250881
hg19250881
hg18250881
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3525515
Samples
Known GenesHS6ST3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039781
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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