A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2765811



Internal ID17518409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:96266345..96272512hg38UCSC Ensembl
Innerchr13:96918599..96924766hg19UCSC Ensembl
Innerchr13:95716600..95722767hg18UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg386168
hg196168
hg186168
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv976262
Supporting Variants
SamplesHGDP01284
Known GenesHS6ST3
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2765811
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer