A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2521n100



Internal ID20154137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:30338750..30488448hg38UCSC Ensembl
chr15:30630953..30780651hg19UCSC Ensembl
chr15:28418245..28567943hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38149699
hg19149699
hg18149699
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1041702, nsv1038902, nsv1053853
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)dgv2521n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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