A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15231007



Internal ID3819855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42428800..42431444hg38UCSC Ensembl
Innerchr15:42428999..42431373hg38UCSC Ensembl
Outerchr15:42428634..42431610hg38UCSC Ensembl
chr15:42720998..42723642hg19UCSC Ensembl
Innerchr15:42721197..42723571hg19UCSC Ensembl
Outerchr15:42720832..42723808hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg382645
hg192645
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636267
Supporting Variants
SamplesHG03458
Known GenesZNF106
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15231007
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer