A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7406



Internal ID15536458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:58974759..58988344hg38UCSC Ensembl
Outerchr18:56641991..56655576hg19UCSC Ensembl
Outerchr18:54792971..54806556hg18UCSC Ensembl
Outerchr18:54792971..54806556hg17UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3813586
hg1913586
hg1813586
hg1713586
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2326
Supporting Variants
SamplesNA12156
Known GenesZNF532
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)nssv7406
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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