A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1049399



Internal ID15555899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:10467520..10528561hg38UCSC Ensembl
Innerchr6:10467753..10528794hg19UCSC Ensembl
Innerchr6:10575739..10636780hg18UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg3861042
hg1961042
hg1861042
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv600981
Supporting Variants
Samples
Known GenesGCNT2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1049399
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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