A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18017296



Internal ID20584336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35579860..35591972hg38UCSC Ensembl
chr14:36049066..36061178hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg3812113
hg1912113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6481165
Supporting Variants
Samples
Known GenesRALGAPA1, RALGAPA1P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18017296
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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