A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576653



Internal ID16017376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:36831639..36935437hg38UCSC Ensembl
Innerchr18:34411602..34515400hg19UCSC Ensembl
Innerchr18:32665600..32769398hg18UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38103799
hg19103799
hg18103799
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv878963
Samples
Known GenesKIAA1328
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576653
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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