A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6202512



Internal ID9622670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24166474..24554599hg38UCSC Ensembl
Outerchr15:24166440..24554634hg38UCSC Ensembl
Innerchr15:24411621..24799746hg19UCSC Ensembl
Outerchr15:24411587..24799781hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38388195
hg19388195
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2672154
Supporting Variants
SamplesNA19332
Known GenesPWRN2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6202512
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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