A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5953953



Internal ID22729221
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 StatusM
Merged Variants
Supporting Variantsnssv17386609
Samples
Known GenesZSCAN20
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5953953
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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