A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054321



Internal ID19143540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:93705414..93725408hg38UCSC Ensembl
Innerchr10:95465171..95485165hg19UCSC Ensembl
Innerchr10:95455161..95475155hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3819995
hg1919995
hg1819995
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3516707
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)nsv1054321
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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