A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12351690



Internal ID2353506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:52762755..52797076hg38UCSC Ensembl
chr6:52627553..52661874hg19UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg3834322
hg1934322
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3609005
Supporting Variants
SamplesHG01164
Known GenesGSTA1, GSTA2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12351690
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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