A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5924169



Internal ID22699396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:95709617..95736498hg38UCSC Ensembl
chr7:95338929..95365810hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3826882
hg1926882
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444689
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5924169
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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