A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17711798



Internal ID135464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:16560433..17214455hg38UCSC Ensembl
chr17:16463747..17117769hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38654023
hg19654023
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6147468
Supporting Variants
Samples
Known GenesCCDC144A, FAM106CP, FLCN, KRT16P2, MPRIP, PLD6, TNFRSF13B, USP32P1, ZNF287, ZNF624
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17711798
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.008586


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