A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1155799



Internal ID15853192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167943158..168191454hg38UCSC Ensembl
Innerchr6:168343838..168592134hg19UCSC Ensembl
Innerchr6:168086687..168334983hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38248297
hg19248297
hg18248297
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605414
Supporting Variants
Samples1780846005_A
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)nssv1155799
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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