A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6545726



Internal ID9656099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2345485..2345664hg38UCSC Ensembl
chr16:2395486..2395665hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38180
hg19180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2673708
Supporting Variants
SamplesNA19385
Known GenesABCA17P
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6545726
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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