A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040531



Internal ID19129750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:110363200..110384646hg38UCSC Ensembl
Innerchr10:112122958..112144404hg19UCSC Ensembl
Innerchr10:112112948..112134394hg18UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3821447
hg1921447
hg1821447
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3706237
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)nsv1040531
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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