A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3567



Internal ID15538295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:112991864..113027147hg38UCSC Ensembl
Outerchr7:112631919..112667202hg19UCSC Ensembl
Outerchr7:112419155..112454438hg18UCSC Ensembl
Outerchr7:112225870..112261153hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg384454
hg194454
hg184454
hg174454
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5906
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)nssv3567
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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