A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033853



Internal ID19123074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143747111..143881082hg38UCSC Ensembl
Innerchr7:143444204..143578175hg19UCSC Ensembl
Innerchr7:143075137..143209108hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38133972
hg19133972
hg18133972
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6717n100
Supporting Variantsnssv3670983, nssv3670984
Samples
Known GenesCTAGE6, FAM115A, LOC154761
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033853
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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