A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3651



Internal ID15538379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:57061853..57076322hg38UCSC Ensembl
Outerchr8:57974412..57988881hg19UCSC Ensembl
Outerchr8:58136966..58151435hg18UCSC Ensembl
Outerchr8:58136966..58151435hg17UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg385518
hg195518
hg185518
hg175518
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6205
Supporting Variants
SamplesNA12878
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)nssv3651
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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