A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573962



Internal ID20947033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:53033215..53033922hg38UCSC Ensembl
chr5:52329045..52329752hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38708
hg19708
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18269046
Samples
Known GenesITGA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573962
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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