A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv656



Internal ID15545210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:94431551..94464013hg38UCSC Ensembl
Outerchr7:94060863..94093325hg19UCSC Ensembl
Outerchr7:93898799..93931261hg18UCSC Ensembl
Outerchr7:93705514..93737976hg17UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg388535
hg198535
hg188535
hg178535
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5850
Supporting Variants
SamplesNA19240
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)nssv656
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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