A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530652



Internal ID20904013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:81965405..82127093hg38UCSC Ensembl
chr17:79923281..80084969hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38161689
hg19161689
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180840
Samples
Known GenesASPSCR1, CCDC57, DCXR, DUS1L, FASN, GPS1, LRRC45, RAC3, RFNG, STRA13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530652
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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