A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038755



Internal ID19127974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:57312127..57401653hg38UCSC Ensembl
Innerchr10:59071887..59161413hg19UCSC Ensembl
Innerchr10:58741893..58831419hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3889527
hg1989527
hg1889527
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3707145
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)nsv1038755
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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