A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17607280



Internal ID21799327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:39001521..39001605hg38UCSC Ensembl
chr14:39470725..39470809hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6023782
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17607280
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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