A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3650363



Internal ID18948644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:149649..217536hg38UCSC Ensembl
Innerchr6:149649..217536hg19UCSC Ensembl
Innerchr6:94649..162536hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3867888
hg1967888
hg1867888
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1016123
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)nssv3650363
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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