A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6346380



Internal ID21003933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:17037201..17066000hg38UCSC Ensembl
chr2:17218468..17247267hg19UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg3828800
hg1928800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18080315
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6346380
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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