A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5567



Internal ID15550389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:160575874..160663627hg38UCSC Ensembl
Outerchr6:160996906..161084659hg19UCSC Ensembl
Outerchr6:160916896..161004649hg18UCSC Ensembl
Outerchr6:160967317..161055070hg17UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3887754
hg1987754
hg1887754
hg1787754
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv596, nssv6101, nssv10524, nssv2624
SamplesNA12156, NA18956, NA18555, NA19240
Known GenesLPA
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)nsv5567
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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