A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5828262



Internal ID22603197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:159889654..159914074hg38UCSC Ensembl
chr1:159859444..159883864hg19UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg3824421
hg1924421
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17466700
Samples
Known GenesCCDC19
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5828262
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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