A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15704229



Internal ID21376505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:106093545..106093882hg38UCSC Ensembl
chr7:105733991..105734328hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4388643
Supporting Variants
Samples
Known GenesSYPL1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15704229
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.525862


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