A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15724735



Internal ID2773329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:64225060..64226959hg38UCSC Ensembl
Innerchr17:64225110..64226909hg38UCSC Ensembl
Outerchr17:64224978..64227041hg38UCSC Ensembl
chr17:62302420..62304319hg19UCSC Ensembl
Innerchr17:62302470..62304269hg19UCSC Ensembl
Outerchr17:62302338..62304401hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3641026
Supporting Variants
SamplesHG02445
Known GenesTEX2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15724735
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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