A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3655757



Internal ID18607352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:27509947..27638063hg38UCSC Ensembl
Innerchr6:27477726..27605842hg19UCSC Ensembl
Innerchr6:27585705..27713821hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38128117
hg19128117
hg18128117
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1030256
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3655757
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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