A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003863



Internal ID18746394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:215383582..215728283hg38UCSC Ensembl
Innerchr2:216248305..216593006hg19UCSC Ensembl
Innerchr2:215956550..216301251hg18UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38344702
hg19344702
hg18344702
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4173n100
Supporting Variantsnssv3585692
Samples
Known GenesFN1, LINC00607
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1003863
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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