A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539936



Internal ID20913231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:234214310..234215727hg38UCSC Ensembl
chr2:235122954..235124371hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg381418
hg191418
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4317n223
Supporting Variantsnssv18257383
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539936
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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