A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067034



Internal ID19156253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:41266750..41282098hg38UCSC Ensembl
Innerchr17:39423002..39438350hg19UCSC Ensembl
Innerchr17:36676528..36691876hg18UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3815349
hg1915349
hg1815349
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3544172, nssv3544173, nssv3544171
Samples
Known GenesKRTAP9-7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1067034
Frequency
Sample Size11257
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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