A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17502626



Internal ID22560567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149123698..149128419hg38UCSC Ensembl
chr7:148820790..148825511hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg384722
hg194722
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5855556
Supporting Variants
Samples
Known GenesZNF398, ZNF425
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17502626
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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