A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8941n54



Internal ID22776836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:7042597..7044033hg38UCSC Ensembl
chr4:7044324..7045760hg19UCSC Ensembl
chr4:7095225..7096661hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg381437
hg191437
hg181437
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv593557, nsv593552, nsv593554, nsv593553, nsv593555, nsv593551
Samples
Known GenesCCDC96, LOC100129931, TADA2B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8941n54
Frequency
Sample Size17421
Observed Gain17
Observed Loss0
Observed Complex0
Frequencyn/a


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