A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv544879



Internal ID16332288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:694362..762550hg38UCSC Ensembl
Innerchr1:629742..697930hg19UCSC Ensembl
Innerchr1:619605..687793hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3868189
hg1968189
hg1868189
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv707629
Samples
Known GenesLOC100133331
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv544879
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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