A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6344896



Internal ID21002449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:103155783..103161406hg38UCSC Ensembl
chr2:103772241..103777864hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg385624
hg195624
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18075147
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6344896
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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