A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6354446



Internal ID21011999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:70155010..70157182hg38UCSC Ensembl
chr2:70382142..70384314hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg382173
hg192173
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18088925
Samples
Known GenesC2orf42
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6354446
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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