A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6752



Internal ID15190426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:35445950..35492054hg38UCSC Ensembl
Outerchr18:33025914..33072018hg19UCSC Ensembl
Outerchr18:31279912..31326016hg18UCSC Ensembl
Outerchr18:31279912..31326016hg17UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3846105
hg1946105
hg1846105
hg1746105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2252
Supporting Variants
SamplesNA12156
Known GenesINO80C
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)nssv6752
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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