A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603752



Internal ID16391161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:74122808..74142296hg38UCSC Ensembl
Innerchr6:74832524..74852012hg19UCSC Ensembl
Innerchr6:74889244..74908732hg18UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3819489
hg1919489
hg1819489
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10783n54
Supporting Variantsnssv1064484, nssv1064485
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603752
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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