A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552102



Internal ID20925232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:59132539..59133084hg38UCSC Ensembl
chr1:59598211..59598756hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg38546
hg19546
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250430
Samples
Known GenesHSD52
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552102
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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