A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12315772



Internal ID4677429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35554207..35601118hg38UCSC Ensembl
chr6:35521984..35568895hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3846912
hg1946912
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3608684
Supporting Variants
SamplesHG04202
Known GenesFKBP5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12315772
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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