A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536247



Internal ID20909600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:105605637..105606050hg38UCSC Ensembl
chr2:106222094..106222507hg19UCSC Ensembl
Cytoband2q12.2
Allele length
AssemblyAllele length
hg38414
hg19414
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18255660
Samples
Known GenesLOC285000
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536247
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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