A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17985994



Internal ID20553034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97386839..97394974hg38UCSC Ensembl
chr10:99146596..99154731hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg388136
hg198136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6446676
Supporting Variants
Samples
Known GenesRRP12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17985994
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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