A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1155794



Internal ID15877210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:150016929..150036876hg38UCSC Ensembl
Innerchr6:150338065..150358012hg19UCSC Ensembl
Innerchr6:150379758..150399705hg18UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3819948
hg1919948
hg1819948
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604847
Supporting Variants
SamplesHGDP00950
Known GenesRAET1L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1155794
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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