A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10567



Internal ID15542231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:96824161..96855449hg38UCSC Ensembl
Outerchr7:96453473..96484761hg19UCSC Ensembl
Outerchr7:96291409..96322697hg18UCSC Ensembl
Outerchr7:96098124..96129412hg17UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3831289
hg1931289
hg1831289
hg1731289
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5857
Supporting Variants
SamplesNA18956
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)nssv10567
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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