A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022295



Internal ID19111513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:6814467..7131745hg38UCSC Ensembl
Innerchr7:6854098..7171376hg19UCSC Ensembl
Innerchr7:6820623..7137901hg18UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38317279
hg19317279
hg18317279
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6245n100
Supporting Variantsnssv3655079
Samples
Known GenesCCZ1B, LOC100131257
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022295
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