A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17421658



Internal ID22479528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:66018447..66018599hg38UCSC Ensembl
chr5:65314275..65314427hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5889628
Supporting Variants
Samples
Known GenesERBB2IP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17421658
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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