A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154819



Internal ID22085324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:27942560..27944711hg38UCSC Ensembl
Outerchr12:27941988..27950527hg38UCSC Ensembl
Innerchr12:28095493..28097644hg19UCSC Ensembl
Outerchr12:28094921..28103460hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg388540
hg198540
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4008985, nssv4008964, nssv4008972, nssv4008987, nssv4008976, nssv4008994, nssv4008993, nssv4008975, nssv4008970, nssv4008962, nssv4008974, nssv4008979, nssv4008981, nssv4008988, nssv4008986, nssv4008963, nssv4008991, nssv4008978, nssv4008982, nssv4008990, nssv4008977, nssv4008984, nssv4008961, nssv4008971, nssv4008973, nssv4008966, nssv4008965, nssv4008992, nssv4008980, nssv4008969, nssv4008967, nssv4008989, nssv4008968, nssv4008983
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154819
Frequency
Sample Size131
Observed Gain0
Observed Loss34
Observed Complex0
Frequencyn/a


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