A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15702896



Internal ID4011669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:55491695..55502591hg38UCSC Ensembl
Innerchr17:55491695..55502591hg38UCSC Ensembl
Outerchr17:55491529..55502741hg38UCSC Ensembl
chr17:53569056..53579952hg19UCSC Ensembl
Innerchr17:53569056..53579952hg19UCSC Ensembl
Outerchr17:53568890..53580102hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3810897
hg1910897
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3640842
Supporting Variants
SamplesHG03667
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15702896
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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