A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027453



Internal ID18769985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:21878856..21942830hg38UCSC Ensembl
Innerchr7:21918474..21982448hg19UCSC Ensembl
Innerchr7:21884999..21948973hg18UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3863975
hg1963975
hg1863975
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643274, nssv3643275
Samples
Known GenesCDCA7L, DNAH11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027453
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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