A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1155800



Internal ID15880818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167943158..168195571hg38UCSC Ensembl
Innerchr6:168343838..168596251hg19UCSC Ensembl
Innerchr6:168086687..168339100hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38252414
hg19252414
hg18252414
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605416
Supporting Variants
SamplesNINDS_33
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)nssv1155800
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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