A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952366



Internal ID16954553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:74429862..74456261hg38UCSC Ensembl
Outerchr17:72426001..72452400hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3826400
hg1926400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998799
SamplesBILGI_BIOE
Known GenesGPRC5C
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952366
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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