A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14098830



Internal ID21267748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:7845484..7857101hg38UCSC Ensembl
Innerchr17:7748802..7760419hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3811618
hg1911618
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110325
Supporting Variants
Samplessample116
Known GenesKDM6B, LSMD1, TMEM88
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14098830
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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