A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028736



Internal ID19117954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:91652391..91714074hg38UCSC Ensembl
Innerchr6:92362109..92423792hg19UCSC Ensembl
Innerchr6:92418830..92480513hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3861684
hg1961684
hg1861684
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3648964
Samples
Known GenesCASC6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028736
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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