A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952370



Internal ID16954557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:76526919..76548618hg38UCSC Ensembl
Outerchr17:74523001..74544700hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3821700
hg1921700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998803
SamplesBILGI_BIOE
Known GenesCYGB, PRCD
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952370
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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