A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024381



Internal ID19113598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:91460244..91484857hg38UCSC Ensembl
Innerchr6:92169962..92194575hg19UCSC Ensembl
Innerchr6:92226683..92251296hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3824614
hg1924614
hg1824614
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3648961, nssv3648962
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)nsv1024381
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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