A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604997



Internal ID16392406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:160536082..160667886hg38UCSC Ensembl
Innerchr6:160957114..161088918hg19UCSC Ensembl
Innerchr6:160877104..161008908hg18UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38131805
hg19131805
hg18131805
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1075169
Samples
Known GenesLPA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604997
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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