A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059422



Internal ID18801953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:73548042..73590244hg38UCSC Ensembl
Innerchr17:71544181..71586383hg19UCSC Ensembl
Innerchr17:69055776..69097978hg18UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3842203
hg1942203
hg1842203
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3567774
Samples
Known GenesSDK2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059422
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer