A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046150



Internal ID19135369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:95105324..95125577hg38UCSC Ensembl
Innerchr10:96865081..96885334hg19UCSC Ensembl
Innerchr10:96855071..96875324hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3820254
hg1920254
hg1820254
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv962n100
Supporting Variantsnssv3517807
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)nsv1046150
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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