A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028512



Internal ID19117730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:123949418..124034313hg38UCSC Ensembl
Innerchr6:124270563..124355458hg19UCSC Ensembl
Innerchr6:124312262..124397157hg18UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3884896
hg1984896
hg1884896
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6143n100
Supporting Variantsnssv3654350
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)nsv1028512
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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