A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1154307



Internal ID15853490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:38907976..38933460hg38UCSC Ensembl
Innerchr6:38875752..38901236hg19UCSC Ensembl
Innerchr6:38983730..39009214hg18UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3825485
hg1925485
hg1825485
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602961
Supporting Variants
Samples1780854231_A
Known GenesDNAH8, LOC100131047
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1154307
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