A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997591



Internal ID19157127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:89365010..89900203hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg18535194
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3965n100
Supporting Variantsnssv3582559, nssv3582561, nssv3582560
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)nsv997591
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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