A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18117265



Internal ID20684305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:48064255..48067831hg38UCSC Ensembl
chr4:48066272..48069848hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg383577
hg193577
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6384615
Supporting Variants
Samples
Known GenesTXK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18117265
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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