A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6336895



Internal ID20994448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:163639061..163639629hg38UCSC Ensembl
chr2:164495571..164496139hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg38569
hg19569
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18079596
Samples
Known GenesFIGN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6336895
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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