A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017751



Internal ID19106968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:75703688..75777782hg38UCSC Ensembl
Innerchr7:75333006..75407100hg19UCSC Ensembl
Innerchr7:75170942..75245036hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3874095
hg1974095
hg1874095
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6468n100
Supporting Variantsnssv3755328
Samples
Known GenesCCL26, HIP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017751
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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