A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025794



Internal ID19115011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:91276024..91407091hg38UCSC Ensembl
Innerchr6:91985742..92116809hg19UCSC Ensembl
Innerchr6:92042463..92173530hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38131068
hg19131068
hg18131068
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6090n100
Supporting Variantsnssv3648959, nssv3648958, nssv3750124
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)nsv1025794
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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