A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5846217



Internal ID22621152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2921081..2936892hg38UCSC Ensembl
chr7:2960715..2976526hg19UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg3815812
hg1915812
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17505386, nssv17505387
Samples
Known GenesCARD11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5846217
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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