A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17839007



Internal ID22022650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:75928799..75928799hg38UCSC Ensembl
chr7:75558117..75558117hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6245411
Supporting Variants
Samples
Known GenesPOR
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17839007
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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