A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5877613



Internal ID22652578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78576788..78598072hg38UCSC Ensembl
chr17:76572870..76594154hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3821285
hg1921285
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17476482
Samples
Known GenesDNAH17
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5877613
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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