A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6550321



Internal ID20923470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:175163919..175164871hg38UCSC Ensembl
chr2:176028647..176029599hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg38953
hg19953
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18256167
Samples
Known GenesATF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6550321
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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