A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550776



Internal ID15991499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46224041..46281263hg38UCSC Ensembl
Innerchr10:47595277..47652499hg19UCSC Ensembl
Innerchr10:47065283..47122505hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3857223
hg1957223
hg1857223
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1114n54
Supporting Variantsnssv1174510, nssv1174509
SamplesNINDS_233, NINDS_51
Known GenesANTXRLP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550776
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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