A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15103387



Internal ID2012776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:95294501..95303095hg38UCSC Ensembl
Innerchr14:95294571..95303026hg38UCSC Ensembl
Outerchr14:95294432..95303165hg38UCSC Ensembl
chr14:95760838..95769432hg19UCSC Ensembl
Innerchr14:95760908..95769363hg19UCSC Ensembl
Outerchr14:95760769..95769502hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg388595
hg198595
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635399
Supporting Variants
SamplesHG01857
Known GenesCLMN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15103387
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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