A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9972



Internal ID15540068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:14791963..14833500hg38UCSC Ensembl
Outerchr18:14791962..14833499hg19UCSC Ensembl
Outerchr18:14781962..14823499hg18UCSC Ensembl
Outerchr18:14781962..14823499hg17UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3841538
hg1941538
hg1841538
hg1741538
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2216
Supporting Variants
SamplesNA18507
Known GenesANKRD30B, MIR3156-2
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)nssv9972
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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