A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17499149



Internal ID22557084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:25127702..25128701hg38UCSC Ensembl
chr5:25127811..25128810hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5842031
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17499149
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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