A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997287



Internal ID19156825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:41052084..41103534hg38UCSC Ensembl
Innerchr3:41093575..41145025hg19UCSC Ensembl
Innerchr3:41068579..41120029hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3851451
hg1951451
hg1851451
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4722n100
Supporting Variantsnssv3589697, nssv3739704, nssv3739703, nssv3739702, nssv3589696, nssv3589695, nssv3589699, nssv3589698, nssv3739705, nssv3589700, nssv3589701
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)nsv997287
Frequency
Sample Size11257
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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