A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550770



Internal ID15991493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46216824..46279254hg38UCSC Ensembl
Innerchr10:47588060..47650490hg19UCSC Ensembl
Innerchr10:47058066..47120496hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3862431
hg1962431
hg1862431
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1114n54
Supporting Variantsnssv747544, nssv1174504
Samples1780854449_A
Known GenesANTXRLP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550770
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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