A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1074982



Internal ID15928168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:156872116..156886388hg38UCSC Ensembl
Innerchr6:157193250..157207522hg19UCSC Ensembl
Innerchr6:157234942..157249214hg18UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3814273
hg1914273
hg1814273
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604976
Supporting Variants
Samples
Known GenesARID1B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1074982
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