A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17375511



Internal ID22601180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21042351..21042407hg38UCSC Ensembl
chr14:21510510..21510566hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5941745
Supporting Variants
Samples
Known GenesNDRG2, RNASE7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17375511
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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