A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18096639



Internal ID20663679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:151724978..151725926hg38UCSC Ensembl
chr3:151442766..151443714hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38949
hg19949
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6372650
Supporting Variants
Samples
Known GenesMIR548H2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18096639
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00026


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