A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17404964



Internal ID22462834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15018732..15018732hg38UCSC Ensembl
chr19:15129544..15129544hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38234
hg19234
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5968974
Supporting Variants
Samples
Known GenesCCDC105
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17404964
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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