A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8234



Internal ID15188944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:36503687..36548342hg38UCSC Ensembl
Outerchr6:36471464..36516119hg19UCSC Ensembl
Outerchr6:36579442..36624097hg18UCSC Ensembl
Outerchr6:36579442..36624097hg17UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3844656
hg1944656
hg1844656
hg1744656
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5260
Supporting Variants
SamplesNA12156
Known GenesSTK38
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)nssv8234
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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