A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5006



Internal ID15544011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:96843485..96855437hg38UCSC Ensembl
Outerchr7:96472797..96484749hg19UCSC Ensembl
Outerchr7:96310733..96322685hg18UCSC Ensembl
Outerchr7:96117448..96129400hg17UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3811953
hg1911953
hg1811953
hg1711953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5857
Supporting Variants
SamplesNA19129
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)nssv5006
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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