A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012638



Internal ID19101855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:6680357..6716927hg38UCSC Ensembl
Innerchr3:6722044..6758614hg19UCSC Ensembl
Innerchr3:6697044..6733614hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3836571
hg1936571
hg1836571
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3739586
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)nsv1012638
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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