A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022455



Internal ID19111673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:150406111..150434797hg38UCSC Ensembl
Innerchr6:150727247..150755933hg19UCSC Ensembl
Innerchr6:150768940..150797626hg18UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3828687
hg1928687
hg1828687
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3749560
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)nsv1022455
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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