A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591938



Internal ID20965009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:43440187..43440824hg38UCSC Ensembl
chr12:43833990..43834627hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg38638
hg19638
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233960
Samples
Known GenesADAMTS20
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591938
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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