A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552340



Internal ID20925467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:33879969..33881683hg38UCSC Ensembl
chr1:34345570..34347284hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg381715
hg191715
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250887
Samples
Known GenesCSMD2, LOC402779
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552340
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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