A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17080882



Internal ID21454499
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 StatusS
Merged Variantsnsv5658769
Supporting Variants
SamplesHG02011
Known GenesSUZ12
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17080882
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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