A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212777



Internal ID20779817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1756795..1912873hg38UCSC Ensembl
chr4:1758522..1914600hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38156079
hg19156079
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6370178
Supporting Variants
Samples
Known GenesFGFR3, LETM1, WHSC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212777
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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