A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606975



Internal ID16394384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:51527709..51547808hg38UCSC Ensembl
Innerchr7:51595406..51615505hg19UCSC Ensembl
Innerchr7:51562900..51582999hg18UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg3820100
hg1920100
hg1820100
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11341n54
Supporting Variantsnssv1084562, nssv1084555, nssv1084559, nssv1084560, nssv1084564, nssv1084563, nssv1084554, nssv1084561, nssv1084558, nssv1084553, nssv1084557, nssv1084556
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606975
Frequency
Sample Size17421
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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