A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537254



Internal ID20910593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:56672315..56673192hg38UCSC Ensembl
chr1:57137988..57138865hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg38878
hg19878
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249838
Samples
Known GenesPRKAA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537254
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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