A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9397n54



Internal ID20142821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:173169007..173169969hg38UCSC Ensembl
chr4:174090158..174091120hg19UCSC Ensembl
chr4:174326733..174327695hg18UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38963
hg19963
hg18963
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv596229, nsv596225, nsv596226, nsv596227, nsv596231, nsv596228, nsv596230
Samples
Known GenesGALNT7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9397n54
Frequency
Sample Size17421
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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