A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15323488



Internal ID5315900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:94293512..94298427hg38UCSC Ensembl
Innerchr15:94293542..94298397hg38UCSC Ensembl
Outerchr15:94293482..94298457hg38UCSC Ensembl
chr15:94836741..94841656hg19UCSC Ensembl
Innerchr15:94836771..94841626hg19UCSC Ensembl
Outerchr15:94836711..94841686hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg384916
hg194916
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637312
Supporting Variants
SamplesNA18864
Known GenesMCTP2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15323488
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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