A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552286



Internal ID16339695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:124528994..124544514hg38UCSC Ensembl
Innerchr10:126217563..126233083hg19UCSC Ensembl
Innerchr10:126207553..126223073hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3815521
hg1915521
hg1815521
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174575
SamplesNINDS_174
Known GenesLHPP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552286
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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