A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2519n100



Internal ID20154135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:30333873..30529543hg38UCSC Ensembl
chr15:30626076..30821746hg19UCSC Ensembl
chr15:28413368..28609038hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38195671
hg19195671
hg18195671
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1038548, nsv1041127, nsv1048601, nsv1049759, nsv1043647, nsv1040948, nsv1040851, nsv1039159, nsv1035451, nsv1042973
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)dgv2519n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss23
Observed Complex0
Frequencyn/a


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