A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034346



Internal ID18776880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:146629723..146670701hg38UCSC Ensembl
Innerchr7:146326815..146367793hg19UCSC Ensembl
Innerchr7:145957748..145998726hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3840979
hg1940979
hg1840979
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3674217
Samples
Known GenesCNTNAP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034346
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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