A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9937n54



Internal ID22777832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:97599035..97766112hg38UCSC Ensembl
chr5:96934739..97101816hg19UCSC Ensembl
chr5:96960495..97127572hg18UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38167078
hg19167078
hg18167078
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv598966, nsv598965, nsv598967
Samples
Known GenesLOC102546227
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9937n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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