A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17386609



Internal ID22444479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:33494103..33494103hg38UCSC Ensembl
chr1:33959703..33959703hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5953953
Supporting Variants
Samples
Known GenesZSCAN20
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17386609
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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