A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17449469



Internal ID22507339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149492764..149617037hg38UCSC Ensembl
chr7:149189855..149314128hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38124274
hg19124274
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5921287
Supporting Variants
Samples
Known GenesZNF746, ZNF767
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17449469
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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