A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15330628



Internal ID6243613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:96807088..96838105hg38UCSC Ensembl
Innerchr15:96807088..96838105hg38UCSC Ensembl
Outerchr15:96806588..96838605hg38UCSC Ensembl
chr15:97350318..97381335hg19UCSC Ensembl
Innerchr15:97350318..97381335hg19UCSC Ensembl
Outerchr15:97349818..97381835hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3831018
hg1931018
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637358
Supporting Variants
SamplesNA19770
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15330628
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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