A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17977996



Internal ID20545036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12421510..12427700hg38UCSC Ensembl
chr10:12463509..12469699hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg386191
hg196191
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6450998
Supporting Variants
Samples
Known GenesCAMK1D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17977996
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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