A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5949413



Internal ID22724862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:88870400..88870400hg38UCSC Ensembl
chr7:88499714..88499714hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17433464
Samples
Known GenesZNF804B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5949413
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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