A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190199



Internal ID20757239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69592739..70157404hg38UCSC Ensembl
chr10:71352495..71917160hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38564666
hg19564666
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6449936
Supporting Variants
Samples
Known GenesAIFM2, C10orf35, COL13A1, H2AFY2, SAR1A, TYSND1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190199
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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