A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5924124



Internal ID22699351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:136789009..136789077hg38UCSC Ensembl
chr7:136473756..136473824hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17438977
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5924124
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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