A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5868400



Internal ID22643335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:8259255..8260954hg38UCSC Ensembl
chr17:8162573..8164272hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17479496
Samples
Known GenesPFAS
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5868400
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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