A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17838461



Internal ID22022104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:38438578..38438578hg38UCSC Ensembl
chr7:38478178..38478178hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38275
hg19275
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6239325
Supporting Variants
Samples
Known GenesAMPH
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17838461
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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