A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577656



Internal ID16018379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:74534683..75005167hg38UCSC Ensembl
Innerchr18:72201918..72717123hg19UCSC Ensembl
Innerchr18:70352898..70846111hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38470485
hg19515206
hg18493214
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv887381
Samples
Known GenesCNDP1, LINC00909, ZNF407
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577656
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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