A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551638



Internal ID16339047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:80453946..80454665hg38UCSC Ensembl
Innerchr10:82213702..82214421hg19UCSC Ensembl
Innerchr10:82203682..82204401hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg38720
hg19720
hg18720
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1291n54
Supporting Variantsnssv751855, nssv751852, nssv751854, nssv751853, nssv751851
Samples
Known GenesTSPAN14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551638
Frequency
Sample Size17421
Observed Gain3
Observed Loss2
Observed Complex0
Frequencyn/a


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