A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153630



Internal ID15508554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:10469593..10528561hg38UCSC Ensembl
Innerchr6:10469826..10528794hg19UCSC Ensembl
Innerchr6:10577812..10636780hg18UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg3858969
hg1958969
hg1858969
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv600984
Supporting Variants
Samples1780862519_A
Known GenesGCNT2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153630
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