A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17433657



Internal ID22491527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:37891470..37897126hg38UCSC Ensembl
chr7:37931072..37936728hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg385657
hg195657
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5922077
Supporting Variants
Samples
Known GenesNME8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17433657
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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