A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054832



Internal ID19144051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:88852009..88938454hg38UCSC Ensembl
Innerchr9:91466924..91553369hg19UCSC Ensembl
Innerchr9:90656744..90743189hg18UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg3886446
hg1986446
hg1886446
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697541
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)nsv1054832
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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