A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849135



Internal ID22624070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133295392..133303074hg38UCSC Ensembl
chr9:136170964..136178557hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg387683
hg197594
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17511685, nssv17511684
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849135
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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