A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6143n100



Internal ID22792230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:123945777..124034313hg38UCSC Ensembl
chr6:124266922..124355458hg19UCSC Ensembl
chr6:124308621..124397157hg18UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3888537
hg1988537
hg1888537
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1031957, nsv1028512, nsv1022439
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)dgv6143n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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