A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997870



Internal ID19157406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:143664689..143892373hg38UCSC Ensembl
Innerchr1:149159329..149386947hg19UCSC Ensembl
Innerchr1:147425953..147653571hg18UCSC Ensembl
Cytoband1q21.1
Allele length
AssemblyAllele length
hg38227685
hg19227619
hg18227619
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv396n100
Supporting Variantsnssv3704189
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)nsv997870
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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