A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551148



Internal ID16338557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:59315453..59380111hg38UCSC Ensembl
Innerchr10:61075213..61139869hg19UCSC Ensembl
Innerchr10:60745219..60809875hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3864659
hg1964657
hg1864657
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174214
Samples1780854039_A
Known GenesFAM13C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551148
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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