A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17506772



Internal ID22564720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:47568093..47587640hg38UCSC Ensembl
chr8:48480655..48500202hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg3819548
hg1919548
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5856887
Supporting Variants
Samples
Known GenesSPIDR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17506772
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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