A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179039



Internal ID20746079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97671807..97847604hg38UCSC Ensembl
chr10:99431564..99607361hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38175798
hg19175798
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6437420
Supporting Variants
Samples
Known GenesAVPI1, LINC00866, MARVELD1, PI4K2A, SFRP5, ZFYVE27
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179039
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00013


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