A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952349



Internal ID16954536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:58318440..58328639hg38UCSC Ensembl
Outerchr17:56395801..56406000hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3810200
hg1910200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998782
SamplesBILGI_BIOE
Known GenesBZRAP1, BZRAP1-AS1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952349
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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