A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6349953



Internal ID21007506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:106821174..106821715hg38UCSC Ensembl
chr2:107437630..107438171hg19UCSC Ensembl
Cytoband2q12.2
Allele length
AssemblyAllele length
hg38542
hg19542
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18076694
Samples
Known GenesST6GAL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6349953
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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