A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009063



Internal ID19098281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:60082140..60291399hg38UCSC Ensembl
Innerchr3:60067866..60277128hg19UCSC Ensembl
Innerchr3:60042906..60252168hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38209260
hg19209263
hg18209263
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4750n100
Supporting Variantsnssv3593400, nssv3593402, nssv3593401, nssv3731128, nssv3731129
Samples
Known GenesFHIT
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009063
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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