A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030389



Internal ID19119608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:73896985..74101990hg38UCSC Ensembl
Innerchr6:74606701..74811706hg19UCSC Ensembl
Innerchr6:74663429..74868426hg18UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38205006
hg19205006
hg18204998
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3658815
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)nsv1030389
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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