A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9918



Internal ID15540002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:128444116..128463152hg38UCSC Ensembl
Outerchr8:129456362..129475398hg19UCSC Ensembl
Outerchr8:129525544..129544580hg18UCSC Ensembl
Outerchr8:129525544..129544580hg17UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3819037
hg1919037
hg1819037
hg1719037
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6391
Supporting Variants
SamplesNA18507
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)nssv9918
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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