A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536794



Internal ID20910137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:42670811..42671271hg38UCSC Ensembl
chr1:43136482..43136942hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38461
hg19461
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250983
Samples
Known GenesPPIH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536794
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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