A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2513n100



Internal ID20154129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:30274687..30488448hg38UCSC Ensembl
chr15:30566890..30780651hg19UCSC Ensembl
chr15:28354182..28567943hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38213762
hg19213762
hg18213762
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1046523, nsv1045992, nsv1053266, nsv1045171, nsv1047880, nsv1035518, nsv1052716, nsv1043679, nsv1047995, nsv1051083
Samples
Known GenesCHRFAM7A, LOC101059918
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2513n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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