A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17509703



Internal ID22567653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:66641966..66644313hg38UCSC Ensembl
chr8:67554201..67556548hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg382348
hg192348
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5859679
Supporting Variants
Samples
Known GenesVCPIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17509703
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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