A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15231174



Internal ID3775276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43598985..43609178hg38UCSC Ensembl
chr15:43891183..43901376hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg3810194
hg1910194
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636291
Supporting Variants
SamplesHG03419
Known GenesCKMT1B, RNU6-28P, STRC
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15231174
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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