A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149697



Internal ID15854158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:11312688..11330718hg38UCSC Ensembl
Innerchr17:11216005..11234035hg19UCSC Ensembl
Innerchr17:11156730..11174760hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3818031
hg1918031
hg1818031
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574361
Supporting Variants
Samples1780862001_A
Known GenesSHISA6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149697
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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