A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1632



Internal ID15546195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:8178349..8223514hg38UCSC Ensembl
Outerchr1:8238409..8283574hg19UCSC Ensembl
Outerchr1:8160996..8206161hg18UCSC Ensembl
Outerchr1:8172675..8217840hg17UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg3845166
hg1945166
hg1845166
hg1745166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7290
SamplesNA12156
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)nsv1632
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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