A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552262



Internal ID16339671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:122585191..122597342hg38UCSC Ensembl
Innerchr10:124344707..124356858hg19UCSC Ensembl
Innerchr10:124334697..124346848hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3812152
hg1912152
hg1812152
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1410n54
Supporting Variantsnssv760449
Samples
Known GenesDMBT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552262
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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