A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019407



Internal ID19108625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:139766170..139983197hg38UCSC Ensembl
Innerchr6:140087307..140304334hg19UCSC Ensembl
Innerchr6:140129000..140346027hg18UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg38217028
hg19217028
hg18217028
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6153n100
Supporting Variantsnssv3654419
Samples
Known GenesLOC100132735
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019407
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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