A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv176n21



Internal ID20131897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:9768841..9772817hg38UCSC Ensembl
chr17:9672158..9676134hg19UCSC Ensembl
chr17:9612883..9616859hg18UCSC Ensembl
chr17:9612883..9616859hg17UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg383977
hg193977
hg183977
hg173977
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv521132, nsv527124
Samples
Known GenesDHRS7C
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv176n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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