A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6348035



Internal ID21005588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:16891123..16933117hg38UCSC Ensembl
chr2:17072390..17114384hg19UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg3841995
hg1941995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18079939
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6348035
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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