A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035111



Internal ID18777642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:142136794..142310364hg38UCSC Ensembl
Innerchr7:141836594..142010187hg19UCSC Ensembl
Innerchr7:141483063..141656682hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38173571
hg19173594
hg18173620
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3667855
Samples
Known GenesLOC730441, LOC93432, MOXD2P, PRSS58
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035111
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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