A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5883601



Internal ID22658583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:37035051..37040500hg38UCSC Ensembl
chr17:35392348..35397798hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg385450
hg195451
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473710
Samples
Known GenesAATF
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5883601
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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