A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997457



Internal ID19156993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75403122..75499571hg38UCSC Ensembl
Innerchr3:75452273..75548722hg19UCSC Ensembl
Innerchr3:75534963..75631412hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3896450
hg1996450
hg1896450
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4782n100
Supporting Variantsnssv3596127, nssv3596128
Samples
Known GenesFAM86DP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv997457
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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