A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10575



Internal ID15542223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:112844175..112881742hg38UCSC Ensembl
Outerchr7:112484230..112521797hg19UCSC Ensembl
Outerchr7:112271466..112309033hg18UCSC Ensembl
Outerchr7:112078181..112115748hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3837568
hg1937568
hg1837568
hg1737568
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5905
Supporting Variants
SamplesNA18956
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)nssv10575
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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