A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997851



Internal ID19157387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:1109220..2002762hg38UCSC Ensembl
Innerchr3:1150904..2044446hg19UCSC Ensembl
Innerchr3:1125904..2019446hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38893543
hg19893543
hg18893543
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4618n100
Supporting Variantsnssv3590297
Samples
Known GenesCNTN6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv997851
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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