A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605376



Internal ID16392785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167933274..168197519hg38UCSC Ensembl
Innerchr6:168333954..168598199hg19UCSC Ensembl
Innerchr6:168076803..168341048hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38264246
hg19264246
hg18264246
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11062n54
Supporting Variantsnssv1077137, nssv1077136, nssv1077135
Samples
Known GenesFRMD1, HGC6.3, KIF25, KIF25-AS1, MLLT4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605376
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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