A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577377



Internal ID16364786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:69006355..69067898hg38UCSC Ensembl
Innerchr18:66673592..66735135hg19UCSC Ensembl
Innerchr18:64824572..64886115hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3861544
hg1961544
hg1861544
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6022n54
Supporting Variantsnssv1150274
SamplesNINDS_223
Known GenesCCDC102B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577377
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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