A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5921287



Internal ID22696510
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 StatusM
Merged Variants
Supporting Variantsnssv17449469
Samples
Known GenesZNF746, ZNF767
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5921287
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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