A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17511574



Internal ID22569526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:131261917..131263016hg38UCSC Ensembl
chr9:134137304..134138403hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5856178
Supporting Variants
Samples
Known GenesFAM78A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17511574
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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