A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155388



Internal ID22085893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:18410516..18561907hg38UCSC Ensembl
Outerchr17:18390113..18565883hg38UCSC Ensembl
Innerchr17:18313830..18465221hg19UCSC Ensembl
Outerchr17:18293427..18469197hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38175771
hg19175771
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv128n97
Supporting Variantsnssv4010122
Samples
Known GenesCCDC144B, FAM106A, FLJ35934, KRT16P1, LGALS9C, LOC339240, USP32P2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155388
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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