A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16263061



Internal ID20472279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:55763051..56019170hg38UCSC Ensembl
chr7:55830744..56086863hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg38256120
hg19256120
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4763959
Supporting Variants
Samples
Known GenesGBAS, MRPS17, PSPH, SEPT14, ZNF713
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16263061
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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