A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5857



Internal ID15550708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:96810852..96864798hg38UCSC Ensembl
Outerchr7:96440164..96494110hg19UCSC Ensembl
Outerchr7:96278100..96332046hg18UCSC Ensembl
Outerchr7:96084815..96138761hg17UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3853947
hg1953947
hg1853947
hg1753947
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9719, nssv5006, nssv2674, nssv10567, nssv3555, nssv11153, nssv660, nssv6151
SamplesNA18507, NA12156, NA12878, NA18956, NA15510, NA18555, NA19240, NA19129
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)nsv5857
Frequency
Sample Size9
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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