A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv670545



Internal ID15060511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167935400..168208655hg38UCSC Ensembl
Innerchr6:168336080..168609335hg19UCSC Ensembl
Innerchr6:168078929..168352184hg18UCSC Ensembl
Innerchr6:168154636..168427891hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38273256
hg19273256
hg18273256
hg17273256
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515568
Supporting Variants
Samples
Known GenesFRMD1, HGC6.3, KIF25, KIF25-AS1, MLLT4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv670545
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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