A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536851



Internal ID20910195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:70171542..70172223hg38UCSC Ensembl
chr2:70398674..70399355hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg38682
hg19682
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258926
Samples
Known GenesC2orf42
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536851
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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