A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5664



Internal ID15550496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:23962980..24008311hg38UCSC Ensembl
Outerchr7:24002599..24047930hg19UCSC Ensembl
Outerchr7:23969124..24014455hg18UCSC Ensembl
Outerchr7:23775839..23821170hg17UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3845332
hg1945332
hg1845332
hg1745332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2638
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)nsv5664
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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