A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17576120



Internal ID21768163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:35674404..35674460hg38UCSC Ensembl
chr7:35714014..35714070hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6010370
Supporting Variants
Samples
Known GenesHERPUD2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17576120
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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