A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600862



Internal ID16388271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:4238254..4472353hg38UCSC Ensembl
Innerchr6:4238488..4472587hg19UCSC Ensembl
Innerchr6:4183487..4417586hg18UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38234100
hg19234100
hg18234100
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10278n54
Supporting Variantsnssv1048711, nssv1048710
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600862
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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