A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576397



Internal ID16017120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:6758922..7036684hg38UCSC Ensembl
Innerchr18:6758921..7036683hg19UCSC Ensembl
Innerchr18:6748921..7026683hg18UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38277763
hg19277763
hg18277763
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv877982
Samples
Known GenesARHGAP28, LAMA1, LINC00668
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576397
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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