A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17571979



Internal ID21764022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:43610095..43616624hg38UCSC Ensembl
chr7:43649694..43656223hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg386530
hg196530
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6008594
Supporting Variants
Samples
Known GenesSTK17A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17571979
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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