A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551187



Internal ID20924324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:231045190..231045719hg38UCSC Ensembl
chr2:231909905..231910434hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg38530
hg19530
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257891
Samples
Known GenesC2orf72
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551187
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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