A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9149



Internal ID15534715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:93758596..93803375hg38UCSC Ensembl
Outerchr13:94410849..94455628hg19UCSC Ensembl
Outerchr13:93208850..93253629hg18UCSC Ensembl
Outerchr13:93208850..93253629hg17UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3844780
hg1944780
hg1844780
hg1744780
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1130
Supporting Variants
SamplesNA12156
Known GenesGPC6
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv9149
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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