A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536431



Internal ID20909779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:40736834..40737621hg38UCSC Ensembl
chr1:41202506..41203293hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38788
hg19788
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250950
Samples
Known GenesNFYC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536431
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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