A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6052371



Internal ID9029774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58620649..58620967hg38UCSC Ensembl
chr15:58912848..58913166hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2675977
Supporting Variants
SamplesHG00707
Known GenesADAM10
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6052371
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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