A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3603878



Internal ID18902159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:130044004..130137891hg38UCSC Ensembl
Innerchr3:129762847..129856734hg19UCSC Ensembl
Innerchr3:131245537..131339424hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3893888
hg1993888
hg1893888
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1013533
Supporting Variants
Samples
Known GenesALG1L2, FAM86HP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3603878
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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