A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5830027



Internal ID22604962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:45616964..45623581hg38UCSC Ensembl
chr1:46082636..46089253hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg386618
hg196618
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463305
Samples
Known GenesCCDC17, NASP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5830027
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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