A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10436



Internal ID15542362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:716502..844631hg38UCSC Ensembl
Outerchr5:716617..844746hg19UCSC Ensembl
Outerchr5:769617..897746hg18UCSC Ensembl
Outerchr5:769617..897746hg17UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38128130
hg19128130
hg18128130
hg17128130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4675
Supporting Variants
SamplesNA18956
Known GenesZDHHC11
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)nssv10436
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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