A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7365



Internal ID15536499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:9247633..9279827hg38UCSC Ensembl
Outerchr18:9247631..9279825hg19UCSC Ensembl
Outerchr18:9237631..9269825hg18UCSC Ensembl
Outerchr18:9237631..9269825hg17UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg3832195
hg1932195
hg1832195
hg1732195
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2201
Supporting Variants
SamplesNA12156
Known GenesANKRD12
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)nssv7365
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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