A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064686



Internal ID19153905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:14994650..15142688hg38UCSC Ensembl
Innerchr17:14897967..15046005hg19UCSC Ensembl
Innerchr17:14838692..14986730hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38148039
hg19148039
hg18148039
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3560381
Samples
Known GenesCDRT7, CDRT8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064686
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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