A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057129



Internal ID19146348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:6203166..6230914hg38UCSC Ensembl
Innerchr17:6106486..6134234hg19UCSC Ensembl
Innerchr17:6047210..6074958hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3827749
hg1927749
hg1827749
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3091n100
Supporting Variantsnssv3560289, nssv3560294, nssv3560290, nssv3560291, nssv3560288, nssv3560293, nssv3560292, nssv3560295
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057129
Frequency
Sample Size11257
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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