A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037136



Internal ID18779667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:14941160..15018277hg38UCSC Ensembl
Innerchr10:14983159..15060276hg19UCSC Ensembl
Innerchr10:15023165..15100282hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3877118
hg1977118
hg1877118
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3707695, nssv3505337, nssv3707694, nssv3504559, nssv3514510, nssv3707696, nssv3707692, nssv3707693
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)nsv1037136
Frequency
Sample Size29084
Observed Gain7
Observed Loss1
Observed Complex0
Frequencyn/a


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