A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016584



Internal ID19105803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:151309223..151343862hg38UCSC Ensembl
Innerchr6:151630358..151664997hg19UCSC Ensembl
Innerchr6:151672051..151706690hg18UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3834640
hg1934640
hg1834640
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6163n100
Supporting Variantsnssv3654473
Samples
Known GenesAKAP12
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016584
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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