A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17498713



Internal ID22556648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:76546787..76551615hg38UCSC Ensembl
chr5:75842612..75847440hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg384829
hg194829
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5843174
Supporting Variants
Samples
Known GenesIQGAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17498713
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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