A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17508311



Internal ID22566260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:60947817..60951609hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg383793
Variant TypeOTHER copy number variation
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5847244
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17508311
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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