A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17425361



Internal ID22483231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:122863948..122864002hg38UCSC Ensembl
chr4:123785103..123785157hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5905599
Supporting Variants
Samples
Known GenesFGF2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17425361
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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