A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545235



Internal ID15985958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:6107849..6109035hg38UCSC Ensembl
Innerchr1:6167909..6169095hg19UCSC Ensembl
Innerchr1:6090496..6091682hg18UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg381187
hg191187
hg181187
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv709149
Samples
Known GenesCHD5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545235
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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