A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041375



Internal ID19130594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:102323590..102364629hg38UCSC Ensembl
Innerchr9:105085872..105126911hg19UCSC Ensembl
Innerchr9:104125693..104166732hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3841040
hg1941040
hg1841040
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3759797
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)nsv1041375
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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