A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600988



Internal ID16041711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:10501021..10614845hg38UCSC Ensembl
Innerchr6:10501254..10615078hg19UCSC Ensembl
Innerchr6:10609240..10723064hg18UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg38113825
hg19113825
hg18113825
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1049413
Samples
Known GenesGCNT2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600988
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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