A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059356



Internal ID19148575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:14636667..15086368hg38UCSC Ensembl
Innerchr17:14539984..14989685hg19UCSC Ensembl
Innerchr17:14480709..14930410hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38449702
hg19449702
hg18449702
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3719179
Samples
Known GenesCDRT7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059356
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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