A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003791



Internal ID18746322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:157650968..157678365hg38UCSC Ensembl
Innerchr1:157620758..157648155hg19UCSC Ensembl
Innerchr1:155887382..155914779hg18UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg3827398
hg1927398
hg1827398
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3485814
Samples
Known GenesFCRL3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1003791
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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