A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5864900



Internal ID22639835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:11703088..11704387hg38UCSC Ensembl
chr8:11560597..11561896hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17505632, nssv17505633
Samples
Known GenesGATA4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5864900
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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