A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17438434



Internal ID22496304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155073841..155073841hg38UCSC Ensembl
chr7:154865551..154865551hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5961963
Supporting Variants
Samples
Known GenesHTR5A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17438434
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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