A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552755



Internal ID20925881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32543791..32544580hg38UCSC Ensembl
chr1:33009392..33010181hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38790
hg19790
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250848
Samples
Known GenesZBTB8A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552755
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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