A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6344605



Internal ID21002158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:55985142..55985934hg38UCSC Ensembl
chr2:56212277..56213069hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg38793
hg19793
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18087631
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6344605
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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