A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6144771



Internal ID343976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:83234700..83247133hg38UCSC Ensembl
chr17:81182469..81194902hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3812434
hg1912434
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17715108
Samples
Known GenesFLJ43681
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6144771
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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