A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550740



Internal ID16338149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46172086..46262954hg38UCSC Ensembl
Innerchr10:47543322..47634190hg19UCSC Ensembl
Innerchr10:47013328..47104196hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3890869
hg1990869
hg1890869
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1107n54
Supporting Variantsnssv747397, nssv747399, nssv747396, nssv747398
Samples
Known GenesANTXRLP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550740
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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