A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1077299



Internal ID15930485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:168314461..168317857hg38UCSC Ensembl
Innerchr6:168715141..168718537hg19UCSC Ensembl
Innerchr6:168457990..168461386hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg383397
hg193397
hg183397
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605460
Supporting Variants
Samples
Known GenesDACT2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1077299
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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