A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553519



Internal ID20926629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:57780771..57781508hg38UCSC Ensembl
chr2:58007906..58008643hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg38738
hg19738
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3890n223
Supporting Variantsnssv18257623
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553519
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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