A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15724800



Internal ID6297766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:65118263..65122393hg38UCSC Ensembl
Innerchr17:65118263..65122393hg38UCSC Ensembl
Outerchr17:65117763..65122893hg38UCSC Ensembl
chr17:63114381..63118511hg19UCSC Ensembl
Innerchr17:63114381..63118511hg19UCSC Ensembl
Outerchr17:63113881..63119011hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg384131
hg194131
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3641036
Supporting Variants
SamplesNA19901
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15724800
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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