A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5846513



Internal ID22621448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:12373128..12374860hg38UCSC Ensembl
chr7:12412754..12414486hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg381733
hg191733
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17509613, nssv17509614
Samples
Known GenesVWDE
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5846513
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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