A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641255



Internal ID7028029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75069337..75071633hg38UCSC Ensembl
Innerchr17:75069383..75071588hg38UCSC Ensembl
Outerchr17:75069292..75071679hg38UCSC Ensembl
chr17:73065432..73067728hg19UCSC Ensembl
Innerchr17:73065478..73067683hg19UCSC Ensembl
Outerchr17:73065387..73067774hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg382297
hg192297
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15740507, essv15740506
SamplesNA19456, NA19475
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641255
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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