A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17505631



Internal ID22563575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:11699724..11709712hg38UCSC Ensembl
chr8:11557233..11567221hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg389989
hg199989
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5859151
Supporting Variants
Samples
Known GenesGATA4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17505631
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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