A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7696



Internal ID15189482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:58451051..58496125hg38UCSC Ensembl
Outerchr20:57026107..57071181hg19UCSC Ensembl
Outerchr20:56459513..56504587hg18UCSC Ensembl
Outerchr20:56459513..56504587hg17UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg3845075
hg1945075
hg1845075
hg1745075
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3428
Supporting Variants
SamplesNA12156
Known GenesAPCDD1L, VAPB
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)nssv7696
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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