A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15740624



Internal ID6833074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75302792..75312510hg38UCSC Ensembl
Innerchr17:75302842..75312460hg38UCSC Ensembl
Outerchr17:75302742..75312560hg38UCSC Ensembl
chr17:73298873..73308591hg19UCSC Ensembl
Innerchr17:73298923..73308541hg19UCSC Ensembl
Outerchr17:73298823..73308641hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg389719
hg199719
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3641262
Supporting Variants
SamplesNA20904
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15740624
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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