A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9762



Internal ID15540084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:37201744..37211800hg38UCSC Ensembl
Outerchr9:37201741..37211797hg19UCSC Ensembl
Outerchr9:37191741..37201797hg18UCSC Ensembl
Outerchr9:37191741..37201797hg17UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg3813259
hg1913259
hg1813259
hg1713259
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6534
Supporting Variants
SamplesNA18507
Known GenesZCCHC7
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)nssv9762
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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