A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18015676



Internal ID20582716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102634133..102637664hg38UCSC Ensembl
chr14:103100470..103104001hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg383532
hg193532
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6500278
Supporting Variants
Samples
Known GenesRCOR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18015676
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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