A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043746



Internal ID19132965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:43445450..43481707hg38UCSC Ensembl
Innerchr10:43940898..43977155hg19UCSC Ensembl
Innerchr10:43260904..43297161hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3836258
hg1936258
hg1836258
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3507297
Samples
Known GenesZNF487
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043746
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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