A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6349253



Internal ID21006806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:15977220..15978870hg38UCSC Ensembl
chr2:16117342..16118992hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg381651
hg191651
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18080504
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6349253
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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