A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5913670



Internal ID22688886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:142309859..142343395hg38UCSC Ensembl
chr7:142009682..142043225hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3833537
hg1933544
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17447095
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5913670
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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