A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5563n100



Internal ID22791650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:7443797..7480778hg38UCSC Ensembl
chr5:7443910..7480891hg19UCSC Ensembl
chr5:7496910..7533891hg18UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3836982
hg1936982
hg1836982
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1034295, nsv1021070
Samples
Known GenesADCY2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5563n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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