A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv760431



Internal ID16054387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:122584630..122598561hg38UCSC Ensembl
Innerchr10:124344146..124358077hg19UCSC Ensembl
Innerchr10:124334136..124348067hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3813932
hg1913932
hg1813932
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552256
Supporting Variants
Samples
Known GenesDMBT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv760431
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer