A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17435656



Internal ID22493526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149157272..149157576hg38UCSC Ensembl
chr7:148854364..148854668hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5911891
Supporting Variants
Samples
Known GenesZNF398
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17435656
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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