A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865905



Internal ID22640840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74495486..74498512hg38UCSC Ensembl
chr7:73909816..73912842hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg383027
hg193027
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17502783
Samples
Known GenesGTF2IRD1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865905
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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