A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7384



Internal ID15536480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:41907077..41951756hg38UCSC Ensembl
Outerchr18:39487042..39531721hg19UCSC Ensembl
Outerchr18:37741040..37785719hg18UCSC Ensembl
Outerchr18:37741040..37785719hg17UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3844680
hg1944680
hg1844680
hg1744680
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2268
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)nssv7384
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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