A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032979



Internal ID19122201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:79175971..79223365hg38UCSC Ensembl
Innerchr7:78805287..78852681hg19UCSC Ensembl
Innerchr7:78643223..78690617hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3847395
hg1947395
hg1847395
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6511n100
Supporting Variantsnssv3657166, nssv3657142, nssv3657134, nssv3657147, nssv3657129, nssv3657163, nssv3657141, nssv3657139, nssv3657135, nssv3657127, nssv3657130, nssv3657125, nssv3657128, nssv3657144, nssv3657151, nssv3657140, nssv3657133, nssv3657149, nssv3657153, nssv3657136, nssv3657148, nssv3657160, nssv3657152, nssv3657138, nssv3657165, nssv3657161, nssv3657143, nssv3657126, nssv3657162, nssv3657146, nssv3657156, nssv3657157, nssv3657154, nssv3657164, nssv3657131, nssv3657132, nssv3657159, nssv3657145, nssv3657158, nssv3657150, nssv3657137, nssv3657155
Samples
Known GenesMAGI2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032979
Frequency
Sample Size11257
Observed Gain0
Observed Loss42
Observed Complex0
Frequencyn/a


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