A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17839104



Internal ID22022747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:130022903..130022903hg38UCSC Ensembl
chr7:129662743..129662743hg19UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6239733
Supporting Variants
Samples
Known GenesZC3HC1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17839104
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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