A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5917019



Internal ID22692238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149146822..149146995hg38UCSC Ensembl
chr7:148843914..148844087hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38174
hg19174
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17440085
Samples
Known GenesZNF398
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5917019
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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