A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610465



Internal ID6650691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:115941259..115955309hg38UCSC Ensembl
Innerchr6:115941259..115955309hg38UCSC Ensembl
Outerchr6:115940759..115955809hg38UCSC Ensembl
chr6:116262422..116276472hg19UCSC Ensembl
Innerchr6:116262422..116276472hg19UCSC Ensembl
Outerchr6:116261922..116276972hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg3814051
hg1914051
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12509734
SamplesHG00452
Known GenesFRK
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610465
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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