A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5856187



Internal ID22631122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:131964203..131965964hg38UCSC Ensembl
chr9:134839590..134841351hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg381762
hg191762
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17511608, nssv17511607
Samples
Known GenesMED27
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5856187
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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