A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6336813



Internal ID20994366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:75214197..75219426hg38UCSC Ensembl
chr2:75441323..75446552hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg385230
hg195230
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18090249
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6336813
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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