A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5699n100



Internal ID22791786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:74402442..74614540hg38UCSC Ensembl
chr5:73698267..73910365hg19UCSC Ensembl
chr5:73734023..73946121hg18UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg38212099
hg19212099
hg18212099
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1018632, nsv1024446
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5699n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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