A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507



Internal ID15551423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:24978825..25003609hg38UCSC Ensembl
Outerchr9:24978823..25003607hg19UCSC Ensembl
Outerchr9:24968823..24993607hg18UCSC Ensembl
Outerchr9:24968823..24993607hg17UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg385961
hg195961
hg185961
hg175961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv794, nssv8595
SamplesNA12156, NA19240
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)nsv6507
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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