A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039128



Internal ID18781659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:74599317..74701249hg38UCSC Ensembl
Innerchr10:76359075..76461007hg19UCSC Ensembl
Innerchr10:76029081..76131013hg18UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38101933
hg19101933
hg18101933
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3507090
Samples
Known GenesADK
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039128
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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