A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608952



Internal ID6995876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:49802958..49838775hg38UCSC Ensembl
chr6:49770671..49806488hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg3835818
hg1935818
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12345028
SamplesHG01413
Known GenesCRISP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608952
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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