A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6345997



Internal ID21003550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:21848724..21849020hg38UCSC Ensembl
chr2:22071596..22071892hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085907
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6345997
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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