A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522672



Internal ID20896033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:77599753..77757348hg38UCSC Ensembl
chr17:75595835..75753430hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38157596
hg19157596
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196870
Samples
Known GenesLOC100132174
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522672
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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