A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6272



Internal ID15190906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:5826402..5870052hg38UCSC Ensembl
Outerchr10:5868365..5912015hg19UCSC Ensembl
Outerchr10:5908371..5952021hg18UCSC Ensembl
Outerchr10:5908371..5952021hg17UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3843651
hg1943651
hg1843651
hg1743651
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5654
Supporting Variants
SamplesNA12156
Known GenesANKRD16
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)nssv6272
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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