A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9726



Internal ID15539966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:110520764..110556337hg38UCSC Ensembl
Outerchr7:110160821..110196394hg19UCSC Ensembl
Outerchr7:109948057..109983630hg18UCSC Ensembl
Outerchr7:109754772..109790345hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3835574
hg1935574
hg1835574
hg1735574
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5897
Supporting Variants
SamplesNA18507
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)nssv9726
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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