A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562634



Internal ID20935705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:42636184..42636695hg38UCSC Ensembl
chr4:42638201..42638712hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg38512
hg19512
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265270
Samples
Known GenesATP8A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562634
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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