A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6301



Internal ID15537562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:135001433..135029709hg38UCSC Ensembl
Outerchr9:137893279..137921555hg19UCSC Ensembl
Outerchr9:137033100..137061376hg18UCSC Ensembl
Outerchr9:135119224..135147500hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg388252
hg198252
hg188252
hg178252
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6755
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)nssv6301
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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