A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568588



Internal ID16355997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:25686278..25687178hg38UCSC Ensembl
Innerchr15:25931425..25932325hg19UCSC Ensembl
Innerchr15:23482518..23483418hg18UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38901
hg19901
hg18901
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4392n54
Supporting Variantsnssv838880, nssv838879, nssv838892, nssv838890, nssv838888, nssv838885, nssv838871, nssv838876, nssv838882, nssv838894, nssv838867, nssv838900, nssv838887, nssv838877, nssv838869, nssv838883, nssv838872, nssv838897, nssv838881, nssv838878, nssv838870, nssv838898, nssv838891, nssv838874, nssv838895, nssv838893, nssv838899, nssv838884, nssv838889, nssv838875, nssv838873, nssv838886, nssv838868, nssv838896
Samples
Known GenesATP10A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568588
Frequency
Sample Size17421
Observed Gain0
Observed Loss34
Observed Complex0
Frequencyn/a


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