A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017603



Internal ID19106820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:19145272..19208993hg38UCSC Ensembl
Innerchr9:19145270..19208991hg19UCSC Ensembl
Innerchr9:19135270..19198991hg18UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3863722
hg1963722
hg1863722
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3690680, nssv3690679, nssv3690678
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)nsv1017603
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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