A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025019



Internal ID19114237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:130753566..130794928hg38UCSC Ensembl
Innerchr6:131074711..131116070hg19UCSC Ensembl
Innerchr6:131116404..131157763hg18UCSC Ensembl
Cytoband6q23.1
Allele length
AssemblyAllele length
hg3841363
hg1941360
hg1841360
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3749539, nssv3654388, nssv3654389, nssv3749538
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)nsv1025019
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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