A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15623560



Internal ID3919916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15072388..15104014hg38UCSC Ensembl
Innerchr17:15072395..15104007hg38UCSC Ensembl
Outerchr17:15072381..15104021hg38UCSC Ensembl
chr17:14975705..15007331hg19UCSC Ensembl
Innerchr17:14975712..15007324hg19UCSC Ensembl
Outerchr17:14975698..15007338hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3831627
hg1931627
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3640054
Supporting Variants
SamplesHG03572
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15623560
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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