A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv707677



Internal ID16001633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:924665..934930hg38UCSC Ensembl
Innerchr1:860045..870310hg19UCSC Ensembl
Innerchr1:849908..860173hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3810266
hg1910266
hg1810266
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv544897
Supporting Variants
Samples
Known GenesSAMD11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv707677
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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