A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007325



Internal ID19096544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:164280481..164376855hg38UCSC Ensembl
Innerchr3:163998269..164094643hg19UCSC Ensembl
Innerchr3:165480963..165577337hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3896375
hg1996375
hg1896375
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4969n100
Supporting Variantsnssv3614540
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007325
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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