A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17434378



Internal ID22492248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155084842..155088915hg38UCSC Ensembl
chr7:154876552..154880625hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg384074
hg194074
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5911608
Supporting Variants
Samples
Known GenesHTR5A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17434378
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.003


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