A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030013



Internal ID19119232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:124655521..124706077hg38UCSC Ensembl
Innerchr6:124976667..125027223hg19UCSC Ensembl
Innerchr6:125018366..125068922hg18UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3850557
hg1950557
hg1850557
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654378
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)nsv1030013
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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