A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6349921



Internal ID21007474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:109015881..109016230hg38UCSC Ensembl
chr2:109632337..109632686hg19UCSC Ensembl
Cytoband2q12.3
Allele length
AssemblyAllele length
hg38350
hg19350
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18075332
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6349921
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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