A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5885405



Internal ID22660389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:29646542..29650254hg38UCSC Ensembl
chr17:27973560..27977272hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg383713
hg193713
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17477550
Samples
Known GenesSSH2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5885405
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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