A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17575663



Internal ID21767706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:55763050..56016250hg38UCSC Ensembl
chr7:55830743..56083943hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg38253201
hg19253201
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6111740
Supporting Variants
Samples
Known GenesGBAS, MRPS17, PSPH, SEPT14, ZNF713
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17575663
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer