A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022439



Internal ID19111657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:123945777..124032966hg38UCSC Ensembl
Innerchr6:124266922..124354111hg19UCSC Ensembl
Innerchr6:124308621..124395810hg18UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3887190
hg1987190
hg1887190
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6143n100
Supporting Variantsnssv3749523
Samples
Known GenesNKAIN2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022439
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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