A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574605



Internal ID20947676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:62360181..62360514hg38UCSC Ensembl
chr5:61656008..61656341hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18269141
Samples
Known GenesKIF2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574605
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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