A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545774



Internal ID16333183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:23610771..23661871hg38UCSC Ensembl
Innerchr1:23937261..23988361hg19UCSC Ensembl
Innerchr1:23809848..23860948hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3851101
hg1951101
hg1851101
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1173799
Samples1780862162_A
Known GenesMDS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545774
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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