A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551929



Internal ID15992652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:92689529..92690255hg38UCSC Ensembl
Innerchr10:94449286..94450012hg19UCSC Ensembl
Innerchr10:94439266..94439992hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38727
hg19727
hg18727
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv753970, nssv753967, nssv753969, nssv753966, nssv753968
Samples
Known GenesHHEX
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551929
Frequency
Sample Size17421
Observed Gain3
Observed Loss2
Observed Complex0
Frequencyn/a


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