A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552267



Internal ID16339676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:122585479..122592081hg38UCSC Ensembl
Innerchr10:124344995..124351597hg19UCSC Ensembl
Innerchr10:124334985..124341587hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg386603
hg196603
hg186603
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1411n54
Supporting Variantsnssv760463, nssv760461, nssv760462, nssv760464, nssv760466, nssv760465
Samples
Known GenesDMBT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552267
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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