A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2651



Internal ID15193773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:55209683..55236938hg38UCSC Ensembl
Outerchr7:55277376..55304631hg19UCSC Ensembl
Outerchr7:55244870..55272125hg18UCSC Ensembl
Outerchr7:55051585..55078840hg17UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3827256
hg1927256
hg1827256
hg1727256
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5755
Supporting Variants
SamplesNA18555
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)nssv2651
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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