A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1155802



Internal ID15853938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167943158..168196562hg38UCSC Ensembl
Innerchr6:168343838..168597242hg19UCSC Ensembl
Innerchr6:168086687..168340091hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38253405
hg19253405
hg18253405
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605417
Supporting Variants
Samples1780854486_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)nssv1155802
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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