A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3653097



Internal ID18951378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:170494093..170532993hg38UCSC Ensembl
Innerchr6:170803181..170842081hg19UCSC Ensembl
Innerchr6:170645106..170684006hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3838901
hg1938901
hg1838901
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1031310
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)nssv3653097
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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