A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970170



Internal ID22745105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:12602785..12602785hg38UCSC Ensembl
chr17:12506102..12506102hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38191
hg19191
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17372212
Samples
Known GenesLINC00670
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970170
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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