A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528



Internal ID15204760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:35666752..35700672hg38UCSC Ensembl
Outerchr9:35666749..35700669hg19UCSC Ensembl
Outerchr9:35656749..35690669hg18UCSC Ensembl
Outerchr9:35656749..35690669hg17UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg385814
hg195814
hg185814
hg175814
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3712
SamplesNA12878
Known GenesCA9, TLN1, TPM2
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)nsv6528
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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