A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610130



Internal ID6650358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:99898771..99938097hg38UCSC Ensembl
chr6:100346647..100385973hg19UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg3839327
hg1939327
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12479367
SamplesNA19700
Known GenesMCHR2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610130
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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