A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540004



Internal ID20913299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:215840697..215841945hg38UCSC Ensembl
chr2:216705420..216706668hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg381249
hg191249
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259280
Samples
Known GenesLINC00607
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540004
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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