A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2649n100



Internal ID22788736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:85745502..85781230hg38UCSC Ensembl
chr15:86288733..86324461hg19UCSC Ensembl
chr15:84089737..84125465hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3835729
hg1935729
hg1835729
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1035162, nsv1042620, nsv1049325, nsv1035336, nsv1048430
Samples
Known GenesAKAP13, KLHL25, MIR1276
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2649n100
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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