A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv878052



Internal ID16172008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:9205190..9206789hg38UCSC Ensembl
Innerchr18:9205188..9206787hg19UCSC Ensembl
Innerchr18:9195188..9196787hg18UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg381600
hg191600
hg181600
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576441
Supporting Variants
Samples
Known GenesANKRD12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv878052
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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