A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554928



Internal ID20928018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35502000..35504186hg38UCSC Ensembl
chr1:35967601..35969787hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg382187
hg192187
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250407
Samples
Known GenesKIAA0319L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554928
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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