A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8484



Internal ID15535380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:20626553..20642205hg38UCSC Ensembl
Outerchr10:20915482..20931134hg19UCSC Ensembl
Outerchr10:20955488..20971140hg18UCSC Ensembl
Outerchr10:20955488..20971140hg17UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3815653
hg1915653
hg1815653
hg1715653
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6021
Supporting Variants
SamplesNA12156
Known Genes
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)nssv8484
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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