A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524550



Internal ID20897911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78134439..78134798hg38UCSC Ensembl
chr17:76130520..76130879hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38360
hg19360
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18038075
Samples
Known GenesTMC8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524550
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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