A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18188537



Internal ID20755577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:88706783..88838563hg38UCSC Ensembl
chr10:90466540..90598320hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38131781
hg19131781
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6440252
Supporting Variants
Samples
Known GenesANKRD22, LIPK, LIPM, LIPN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18188537
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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