A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552677



Internal ID20925803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:74467903..74468890hg38UCSC Ensembl
chr2:74695030..74696017hg19UCSC Ensembl
Cytoband2p13.1
Allele length
AssemblyAllele length
hg38988
hg19988
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258365
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552677
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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