A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575110



Internal ID20948181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:60894268..60894933hg38UCSC Ensembl
chr5:60190095..60190760hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg38666
hg19666
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268945
Samples
Known GenesERCC8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575110
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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