A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006677



Internal ID18749208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:143694184..144572337hg38UCSC Ensembl
Innerchr1:149188835..149521828hg19UCSC Ensembl
Innerchr1:147455459..147788452hg18UCSC Ensembl
Cytoband1q21.1
Allele length
AssemblyAllele length
hg38878154
hg19332994
hg18332994
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv397n100
Supporting Variantsnssv3704209
Samples
Known GenesFCGR1C, LOC388692
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1006677
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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