A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538621



Internal ID20911934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:232707842..232708741hg38UCSC Ensembl
chr2:233572552..233573451hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257361
Samples
Known GenesGIGYF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538621
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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