A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6353607



Internal ID21011160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:16786013..16794047hg38UCSC Ensembl
chr2:16967280..16975314hg19UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg388035
hg198035
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18079320
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6353607
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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