A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7407



Internal ID15536457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:59843729..59877788hg38UCSC Ensembl
Outerchr18:57510961..57545020hg19UCSC Ensembl
Outerchr18:55661941..55696000hg18UCSC Ensembl
Outerchr18:55661941..55696000hg17UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg385374
hg195374
hg185374
hg175374
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2327
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)nssv7407
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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