A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047566



Internal ID19136785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:121675623..121699918hg38UCSC Ensembl
Innerchr10:123435137..123459432hg19UCSC Ensembl
Innerchr10:123425127..123449422hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3824296
hg1924296
hg1824296
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv985n100
Supporting Variantsnssv3518770
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)nsv1047566
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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