A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042205



Internal ID19131424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:9612413..9648732hg38UCSC Ensembl
Innerchr10:9654376..9690695hg19UCSC Ensembl
Innerchr10:9694382..9730701hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3836320
hg1936320
hg1836320
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3707686
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)nsv1042205
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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