A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516645



Internal ID15443938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:9177974..9178308hg38UCSC Ensembl
Innerchr18:9177972..9178306hg19UCSC Ensembl
Innerchr18:9167972..9168306hg18UCSC Ensembl
Innerchr18:9167972..9168306hg17UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38335
hg19335
hg18335
hg17335
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv187n21
Supporting Variantsnssv669845, nssv659012, nssv655182, nssv676659
Samples
Known GenesANKRD12
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516645
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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