A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv707621



Internal ID16001577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:121042..137049hg38UCSC Ensembl
Innerchr1:121042..137049hg19UCSC Ensembl
Innerchr1:110905..126912hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3816008
hg1916008
hg1816008
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv544871
Supporting Variants
Samples
Known GenesLOC729737
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv707621
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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