A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527923



Internal ID20901284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:64618994..64979125hg38UCSC Ensembl
chr17:62615112..62975243hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg38360132
hg19360132
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195479
Samples
Known GenesAMZ2P1, LOC146880, LRRC37A3, MIR4315-1, MIR4315-2, MIR6080, PLEKHM1P, SMURF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527923
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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