A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv878057



Internal ID16172013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:9206005..9211271hg38UCSC Ensembl
Innerchr18:9206003..9211269hg19UCSC Ensembl
Innerchr18:9196003..9201269hg18UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg385267
hg195267
hg185267
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576446
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)nssv878057
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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