A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540604



Internal ID20913893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:57780792..57781651hg38UCSC Ensembl
chr2:58007927..58008786hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg38860
hg19860
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3890n223
Supporting Variantsnssv18257624
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540604
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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