A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028432



Internal ID19117650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:76288541..76307348hg38UCSC Ensembl
Innerchr6:76998258..77017065hg19UCSC Ensembl
Innerchr6:77054978..77073785hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3818808
hg1918808
hg1818808
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3658823, nssv3658822
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)nsv1028432
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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