A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529



Internal ID15551447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:36399228..36406121hg38UCSC Ensembl
Outerchr9:36399225..36406118hg19UCSC Ensembl
Outerchr9:36389225..36396118hg18UCSC Ensembl
Outerchr9:36389225..36396118hg17UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg3829986
hg1929986
hg1829986
hg1729986
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5154
SamplesNA19129
Known GenesRNF38
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)nsv6529
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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