A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047226



Internal ID19136445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:6609465..6622192hg38UCSC Ensembl
Innerchr10:6651427..6664154hg19UCSC Ensembl
Innerchr10:6691433..6704160hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3812728
hg1912728
hg1812728
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv667n100
Supporting Variantsnssv3493691, nssv3485611
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)nsv1047226
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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