A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544883



Internal ID20918121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:34997455..34997953hg38UCSC Ensembl
chr1:35463056..35463554hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38499
hg19499
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250895
Samples
Known GenesZMYM6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544883
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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