A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6337060



Internal ID20994613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:21599231..21635209hg38UCSC Ensembl
chr2:21822103..21858081hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3835979
hg1935979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085750
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6337060
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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