A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5950501



Internal ID22725901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107591641..107591641hg38UCSC Ensembl
chr7:107232086..107232086hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38255
hg19255
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17438455
Samples
Known GenesBCAP29
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5950501
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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