A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550007



Internal ID16337416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:14948370..15018884hg38UCSC Ensembl
Innerchr10:14990369..15060883hg19UCSC Ensembl
Innerchr10:15030375..15100889hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3870515
hg1970515
hg1870515
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv744086, nssv744090, nssv744084, nssv744088, nssv744087, nssv744089, nssv744085, nssv1174133
Samples1780862378_A
Known GenesDCLRE1C, MEIG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550007
Frequency
Sample Size17421
Observed Gain7
Observed Loss1
Observed Complex0
Frequencyn/a


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