A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15748493



Internal ID4389250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:77627800..77656227hg38UCSC Ensembl
Innerchr17:77627827..77656201hg38UCSC Ensembl
Outerchr17:77627774..77656254hg38UCSC Ensembl
chr17:75623882..75652309hg19UCSC Ensembl
Innerchr17:75623909..75652283hg19UCSC Ensembl
Outerchr17:75623856..75652336hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3828428
hg1928428
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3641317
Supporting Variants
SamplesHG03911
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15748493
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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