A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641176



Internal ID7027950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:71685037..71689374hg38UCSC Ensembl
Innerchr17:71685537..71688874hg38UCSC Ensembl
Outerchr17:71684037..71690374hg38UCSC Ensembl
chr17:69681178..69685515hg19UCSC Ensembl
Innerchr17:69681678..69685015hg19UCSC Ensembl
Outerchr17:69680178..69686515hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg384338
hg194338
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15734790
SamplesHG00106
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641176
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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