A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060030



Internal ID19149249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:41354648..41370156hg38UCSC Ensembl
Innerchr17:39510900..39526408hg19UCSC Ensembl
Innerchr17:36764426..36779934hg18UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3815509
hg1915509
hg1815509
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3173n100
Supporting Variantsnssv3545103
Samples
Known GenesKRT33B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060030
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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