A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552324



Internal ID16339733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:130771908..130800011hg38UCSC Ensembl
Innerchr10:132570172..132598275hg19UCSC Ensembl
Innerchr10:132460162..132488265hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3828104
hg1928104
hg1828104
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174585
SamplesNINDS_65
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552324
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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