A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550229



Internal ID16337638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:26559277..26600894hg38UCSC Ensembl
Innerchr10:26848206..26889823hg19UCSC Ensembl
Innerchr10:26888212..26929829hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3841618
hg1941618
hg1841618
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv744740
Samples
Known GenesAPBB1IP, LINC00264
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550229
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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