A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547421



Internal ID20920622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:60911992..60915086hg38UCSC Ensembl
chr2:61139127..61142221hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg383095
hg193095
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257673
Samples
Known GenesREL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547421
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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