A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005690



Internal ID18748221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:41873664..41990202hg38UCSC Ensembl
Innerchr3:41915156..42031694hg19UCSC Ensembl
Innerchr3:41890160..42006698hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38116539
hg19116539
hg18116539
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4726n100
Supporting Variantsnssv3589716
Samples
Known GenesULK4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1005690
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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