A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1729n100



Internal ID22787816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:91769467..91849951hg38UCSC Ensembl
chr13:92421721..92502205hg19UCSC Ensembl
chr13:91219722..91300206hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3880485
hg1980485
hg1880485
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1036226, nsv1053048, nsv1053597
Samples
Known GenesGPC5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1729n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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