A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5905



Internal ID15550761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:112805370..112881742hg38UCSC Ensembl
Outerchr7:112445425..112521797hg19UCSC Ensembl
Outerchr7:112232661..112309033hg18UCSC Ensembl
Outerchr7:112039376..112115748hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3876373
hg1976373
hg1876373
hg1776373
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6162, nssv10575
SamplesNA12156, NA18956
Known GenesC7orf60
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)nsv5905
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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