A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6106



Internal ID15537757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:168224440..168247407hg38UCSC Ensembl
Outerchr6:168625120..168648087hg19UCSC Ensembl
Outerchr6:168367969..168390936hg18UCSC Ensembl
Outerchr6:168443676..168466643hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg388546
hg198546
hg188546
hg178546
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5594
Supporting Variants
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)nssv6106
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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