A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024527



Internal ID19113744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:132211801..132250750hg38UCSC Ensembl
Innerchr6:132532941..132571889hg19UCSC Ensembl
Innerchr6:132574634..132613582hg18UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3838950
hg1938949
hg1838949
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654394
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)nsv1024527
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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