A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057983



Internal ID19147202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:26076647..26197373hg38UCSC Ensembl
Innerchr20:26057283..26178009hg19UCSC Ensembl
Innerchr20:26005283..26126009hg18UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg38120727
hg19120727
hg18120727
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3737188
Samples
Known GenesFAM182A, LOC284801, NCOR1P1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057983
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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