A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18184433



Internal ID20751473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:96976055..97000287hg38UCSC Ensembl
chr10:98735812..98760044hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3824233
hg1924233
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6441601
Supporting Variants
Samples
Known GenesC10orf12, SLIT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18184433
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00013


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