A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571165



Internal ID20944236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:162010248..162012602hg38UCSC Ensembl
chr5:161437254..161439608hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg382355
hg192355
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6007n223
Supporting Variantsnssv18267464
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571165
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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