A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6346526



Internal ID21004079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:205210401..205216400hg38UCSC Ensembl
chr2:206075125..206081124hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg386000
hg196000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18082330
Samples
Known GenesPARD3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6346526
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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