A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv544872



Internal ID16332281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:121042..137674hg38UCSC Ensembl
Innerchr1:121042..137674hg19UCSC Ensembl
Innerchr1:110905..127537hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3816633
hg1916633
hg1816633
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2n54
Supporting Variantsnssv707622
Samples
Known GenesLOC729737
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv544872
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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