A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067369



Internal ID19156588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:41249017..41276460hg38UCSC Ensembl
Innerchr17:39405269..39432712hg19UCSC Ensembl
Innerchr17:36658795..36686238hg18UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3827444
hg1927444
hg1827444
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3161n100
Supporting Variantsnssv3562581
Samples
Known GenesKRTAP9-4, KRTAP9-6, KRTAP9-7, KRTAP9-9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1067369
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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