A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542796



Internal ID20916048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:135191157..135198983hg38UCSC Ensembl
chr2:135948727..135956553hg19UCSC Ensembl
Cytoband2q21.3
Allele length
AssemblyAllele length
hg387827
hg197827
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18255860
Samples
Known GenesZRANB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542796
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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