A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520271



Internal ID20893632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:74787297..74787398hg38UCSC Ensembl
chr17:72783436..72783537hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18038444
Samples
Known GenesTMEM104
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520271
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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