A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6337907



Internal ID20995460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:69861132..69874980hg38UCSC Ensembl
chr2:70088264..70102112hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg3813849
hg1913849
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18088904
Samples
Known GenesGMCL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6337907
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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