A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551914



Internal ID15992637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:91605258..91624316hg38UCSC Ensembl
Innerchr10:93365015..93384073hg19UCSC Ensembl
Innerchr10:93354995..93374053hg18UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg3819059
hg1919059
hg1819059
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv753455
Samples
Known GenesLOC100188947
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551914
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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