A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17509671



Internal ID22567621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:64377094..64378131hg38UCSC Ensembl
chr8:65289651..65290688hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg381038
hg191038
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5866269
Supporting Variants
Samples
Known GenesLINC00966
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17509671
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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