A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5921020



Internal ID22696243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:138981005..138981116hg38UCSC Ensembl
chr7:138665751..138665862hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17437797
Samples
Known GenesKIAA1549
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5921020
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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