A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852684



Internal ID22627619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:70190576..70199769hg38UCSC Ensembl
chr9:72805492..72814685hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg389194
hg199194
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17514183
Samples
Known GenesMAMDC2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852684
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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