A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6337860



Internal ID20995413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:102464929..102479979hg38UCSC Ensembl
chr2:103081389..103096438hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg3815051
hg1915050
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18075107
Samples
Known GenesSLC9A4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6337860
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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