A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5846929



Internal ID22621864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:32574770..32576169hg38UCSC Ensembl
chr7:32614382..32615781hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17505510, nssv17505509
Samples
Known GenesAVL9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5846929
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer