A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047489



Internal ID19136708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:56570760..56722996hg38UCSC Ensembl
Innerchr10:58330520..58482756hg19UCSC Ensembl
Innerchr10:58000526..58152762hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38152237
hg19152237
hg18152237
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv869n100
Supporting Variantsnssv3503943, nssv3519050, nssv3519892
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)nsv1047489
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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