A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17607069



Internal ID21799116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35974929..36025544hg38UCSC Ensembl
chr14:36444135..36494750hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg3850616
hg1950616
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6023210
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17607069
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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