A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9667



Internal ID15540136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:60695393..60743983hg38UCSC Ensembl
Outerchr5:59991220..60039810hg19UCSC Ensembl
Outerchr5:60026977..60075567hg18UCSC Ensembl
Outerchr5:60026977..60075567hg17UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg3848591
hg1948591
hg1848591
hg1748591
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4850
Supporting Variants
SamplesNA18507
Known GenesDEPDC1B
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)nssv9667
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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