A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15745932



Internal ID3635249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76954201..76962602hg38UCSC Ensembl
Innerchr17:76954228..76962576hg38UCSC Ensembl
Outerchr17:76954175..76962629hg38UCSC Ensembl
chr17:74950283..74958684hg19UCSC Ensembl
Innerchr17:74950310..74958658hg19UCSC Ensembl
Outerchr17:74950257..74958711hg19UCSC Ensembl
Cytoband17q25.2
Allele length
AssemblyAllele length
hg388402
hg198402
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3641302
Supporting Variants
SamplesHG03234
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15745932
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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