A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5828342



Internal ID22603277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:14948329..14953080hg38UCSC Ensembl
chr1:15274825..15279576hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg384752
hg194752
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17454278
Samples
Known GenesKAZN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5828342
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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