A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606816



Internal ID16394225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:44960264..44961683hg38UCSC Ensembl
Innerchr7:44999863..45001282hg19UCSC Ensembl
Innerchr7:44966388..44967807hg18UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg381420
hg191420
hg181420
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11313n54
Supporting Variantsnssv1083568
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606816
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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