A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6303669



Internal ID9716276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69961725..69965874hg38UCSC Ensembl
chr15:70254064..70258213hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg384150
hg194150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2674946
Supporting Variants
SamplesNA19469
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6303669
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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