A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017295



Internal ID18759830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:25916355..26001317hg38UCSC Ensembl
Innerchr9:25916353..26001315hg19UCSC Ensembl
Innerchr9:25906353..25991315hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg3884963
hg1984963
hg1884963
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3755871
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)nsv1017295
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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