A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5927088



Internal ID22702316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:134884491..134884583hg38UCSC Ensembl
chr7:134569242..134569334hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17445449
Samples
Known GenesCALD1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5927088
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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