A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041165



Internal ID18783696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:95869767..96314266hg38UCSC Ensembl
Innerchr13:96522021..96966520hg19UCSC Ensembl
Innerchr13:95320022..95764521hg18UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38444500
hg19444500
hg18444500
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3713284
Samples
Known GenesHS6ST3, UGGT2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041165
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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