A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024915



Internal ID19114132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:150086471..150104374hg38UCSC Ensembl
Innerchr6:150407607..150425510hg19UCSC Ensembl
Innerchr6:150449300..150467203hg18UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3817904
hg1917904
hg1817904
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6161n100
Supporting Variantsnssv3654466
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)nsv1024915
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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