A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577095



Internal ID16364504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:62587556..62623811hg38UCSC Ensembl
Innerchr18:60254789..60291044hg19UCSC Ensembl
Innerchr18:58405769..58442024hg18UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg3836256
hg1936256
hg1836256
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150018
SamplesNINDS_61
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577095
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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