A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525776



Internal ID20899137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75111471..75115291hg38UCSC Ensembl
chr17:73107566..73111386hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg383821
hg193821
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192449
Samples
Known GenesARMC7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525776
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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