A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998261



Internal ID18811111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:212856472..212890867hg38UCSC Ensembl
Innerchr1:213029814..213064209hg19UCSC Ensembl
Innerchr1:211096437..211130832hg18UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg3834396
hg1934396
hg1834396
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv572n100
Supporting Variantsnssv3498868
Samples
Known GenesFLVCR1, FLVCR1-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv998261
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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