A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045188



Internal ID18787719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:14936970..15015784hg38UCSC Ensembl
Innerchr10:14978969..15057783hg19UCSC Ensembl
Innerchr10:15018975..15097789hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3878815
hg1978815
hg1878815
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3508015
Samples
Known GenesDCLRE1C, MEIG1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045188
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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