A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17509175



Internal ID22567125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:36203631..36215692hg38UCSC Ensembl
chr8:36061149..36073210hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3812062
hg1912062
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5866134
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17509175
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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