A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6425



Internal ID15204647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:139669711..139716181hg38UCSC Ensembl
Outerchr8:140681954..140728424hg19UCSC Ensembl
Outerchr8:140751136..140797606hg18UCSC Ensembl
Outerchr8:140751136..140797606hg17UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3846471
hg1946471
hg1846471
hg1746471
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6257
SamplesNA12156
Known GenesKCNK9
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)nsv6425
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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