A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440



Internal ID15551350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:143644943..143677285hg38UCSC Ensembl
Outerchr8:144727113..144759455hg19UCSC Ensembl
Outerchr8:144798256..144831443hg18UCSC Ensembl
Outerchr8:144798256..144831443hg17UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg386097
hg196097
hg186097
hg176097
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5140
SamplesNA19129
Known GenesZNF623
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)nsv6440
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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