A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17977999



Internal ID20545039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12425074..12426644hg38UCSC Ensembl
chr10:12467073..12468643hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg381571
hg191571
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6438921
Supporting Variants
Samples
Known GenesCAMK1D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17977999
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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