A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604976



Internal ID16392385
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 StatusM
Merged Variants
Supporting Variantsnssv1074982
Samples
Known GenesARID1B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604976
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