A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028413



Internal ID19117631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143549301..143870954hg38UCSC Ensembl
Innerchr7:143246394..143568047hg19UCSC Ensembl
Innerchr7:142956516..143198980hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38321654
hg19321654
hg18242465
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6706n100
Supporting Variantsnssv3670408
Samples
Known GenesCTAGE15, CTAGE6, FAM115A, FAM115C, LOC154761
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028413
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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