A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953902



Internal ID16956089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:44951533..45058632hg38UCSC Ensembl
Outerchr17:43028901..43136000hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38107100
hg19107100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998748
SamplesBILGI_BIOE
Known GenesC1QL1, DCAKD
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953902
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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