A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17494653



Internal ID22552584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:67728519..67769751hg38UCSC Ensembl
chr3:67778943..67820175hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3841233
hg1941233
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5836463
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17494653
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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