A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841179



Internal ID22616114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:148260917..148304789hg38UCSC Ensembl
chr5:147640480..147684352hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3843873
hg1943873
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17496264
Samples
Known GenesLOC102546294, SPINK13
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841179
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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