A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1048714



Internal ID15901900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:4255474..4464396hg38UCSC Ensembl
Innerchr6:4255708..4464630hg19UCSC Ensembl
Innerchr6:4200707..4409629hg18UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38208923
hg19208923
hg18208923
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv600864
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1048714
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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