A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499984



Internal ID20873209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39637291..39640487hg38UCSC Ensembl
chr17:37793544..37796740hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg383197
hg193197
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196724
Samples
Known GenesSTARD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499984
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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