A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031710



Internal ID19120932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:13987713..14121675hg38UCSC Ensembl
Innerchr8:13845222..13979184hg19UCSC Ensembl
Innerchr8:13889593..14023555hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38133963
hg19133963
hg18133963
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3675853
Samples
Known GenesSGCZ
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031710
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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