A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17509673



Internal ID22567623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:64577066..64579100hg38UCSC Ensembl
chr8:65489623..65491657hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg382035
hg192035
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5849983
Supporting Variants
Samples
Known GenesLOC401463
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17509673
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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