A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510440



Internal ID20883758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:36497701..36503700hg38UCSC Ensembl
chr17:34853545..34859540hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg386000
hg195996
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180509
Samples
Known GenesMYO19, ZNHIT3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510440
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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