A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039655



Internal ID18782186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:17941330..18060025hg38UCSC Ensembl
Innerchr10:18230259..18348954hg19UCSC Ensembl
Innerchr10:18270265..18388960hg18UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg38118696
hg19118696
hg18118696
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3509391
Samples
Known GenesLOC100129213, SLC39A12
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039655
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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