A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17441031



Internal ID22498901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:11739420..11739756hg38UCSC Ensembl
chr8:11596929..11597265hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38337
hg19337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5922515
Supporting Variants
Samples
Known GenesGATA4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17441031
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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