A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999855



Internal ID19159391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:91460974..91602662hg38UCSC Ensembl
Innerchr2:91653350..91790688hg19UCSC Ensembl
Innerchr2:91017077..91154415hg18UCSC Ensembl
Cytoband2p11.1
Allele length
AssemblyAllele length
hg38141689
hg19137339
hg18137339
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3995n100
Supporting Variantsnssv3579451
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv999855
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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