A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17560969



Internal ID21885324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:129475521..129475743hg38UCSC Ensembl
chr7:129115362..129115584hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg38223
hg19223
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6013310
Supporting Variants
Samples
Known GenesSTRIP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17560969
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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