A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17509033



Internal ID22566983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:96887895..96891484hg38UCSC Ensembl
chr6:97335771..97339360hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg383590
hg193590
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5845856
Supporting Variants
Samples
Known GenesNDUFAF4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17509033
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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