A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3697



Internal ID15538425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:141757002..141788161hg38UCSC Ensembl
Outerchr8:142838363..142869522hg19UCSC Ensembl
Outerchr8:142836270..142867429hg18UCSC Ensembl
Outerchr8:142836270..142867429hg17UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg387156
hg197156
hg187156
hg177156
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6435
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)nssv3697
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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