A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607671



Internal ID16048394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:79686445..79773235hg38UCSC Ensembl
Innerchr7:79315761..79402551hg19UCSC Ensembl
Innerchr7:79153697..79240487hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3886791
hg1986791
hg1886791
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11481n54
Supporting Variantsnssv1155212
SamplesHGDP00796
Known GenesMIR548M
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607671
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