A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007857



Internal ID18750388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:138048612..138124264hg38UCSC Ensembl
Innerchr3:137767454..137843106hg19UCSC Ensembl
Innerchr3:139250144..139325796hg18UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3875653
hg1975653
hg1875653
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3608328, nssv3608327
Samples
Known GenesA4GNT, DZIP1L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007857
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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