A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5658769



Internal ID21607074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:31941117..31941117hg38UCSC Ensembl
chr17:30268136..30268136hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38992
hg19992
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17080882
SamplesHG02011
Known GenesSUZ12
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5658769
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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