A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019159



Internal ID19108377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:6814467..6880637hg38UCSC Ensembl
Innerchr7:6854098..6920268hg19UCSC Ensembl
Innerchr7:6820623..6886793hg18UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3866171
hg1966171
hg1866171
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6244n100
Supporting Variantsnssv3655075, nssv3752812
Samples
Known GenesCCZ1B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019159
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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