A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17492797



Internal ID22550725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:20405925..20406924hg38UCSC Ensembl
chr4:20407548..20408547hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5839222
Supporting Variants
Samples
Known GenesSLIT2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17492797
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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