A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604260



Internal ID16044983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:100032919..100216963hg38UCSC Ensembl
Innerchr6:100480795..100664839hg19UCSC Ensembl
Innerchr6:100587516..100771560hg18UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg38184045
hg19184045
hg18184045
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1070556
Samples
Known GenesMCHR2-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604260
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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