A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17577620



Internal ID21769663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:96147254..96147492hg38UCSC Ensembl
chr8:97159482..97159720hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38239
hg19239
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6008508
Supporting Variants
Samples
Known GenesGDF6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17577620
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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