A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548963



Internal ID20922141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:125767924..126452768hg38UCSC Ensembl
chr2:126525501..127210345hg19UCSC Ensembl
Cytoband2q14.3
Allele length
AssemblyAllele length
hg38684845
hg19684845
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18256740
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548963
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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