A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5887136



Internal ID22662128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:81722754..81725465hg38UCSC Ensembl
chr17:79689784..79692495hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg382712
hg192712
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17476525
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5887136
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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