A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043780



Internal ID19132999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:19126646..19538355hg38UCSC Ensembl
Innerchr10:19415575..19827284hg19UCSC Ensembl
Innerchr10:19455581..19867290hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38411710
hg19411710
hg18411710
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv683n100
Supporting Variantsnssv3707700
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)nsv1043780
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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