A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17425844



Internal ID22483714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:60725885..60726148hg38UCSC Ensembl
chr4:61591603..61591866hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg38264
hg19264
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5897608
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17425844
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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