A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv548198



Internal ID16335607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:174762458..174831734hg38UCSC Ensembl
Innerchr1:174731596..174800872hg19UCSC Ensembl
Innerchr1:172998219..173067495hg18UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg3869277
hg1969277
hg1869277
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv728820
Samples
Known GenesRABGAP1L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv548198
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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