A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006339



Internal ID19095557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:7049651..7075009hg38UCSC Ensembl
Innerchr3:7091338..7116696hg19UCSC Ensembl
Innerchr3:7066338..7091696hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3825359
hg1925359
hg1825359
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3591830
Samples
Known GenesGRM7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1006339
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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