A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552772



Internal ID20925899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:202309122..202310639hg38UCSC Ensembl
chr2:203173845..203175362hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg381518
hg191518
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4256n223
Supporting Variantsnssv18257709
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552772
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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