A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6037575



Internal ID9014978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75879289..75883349hg38UCSC Ensembl
chr17:73875370..73879430hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg384061
hg194061
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2666227
Supporting Variants
SamplesNA19360
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6037575
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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