A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034992



Internal ID19124211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:119191492..119219730hg38UCSC Ensembl
Innerchr6:119512657..119540895hg19UCSC Ensembl
Innerchr6:119554356..119582594hg18UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3828239
hg1928239
hg1828239
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654334
Samples
Known GenesMAN1A1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034992
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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