A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526401



Internal ID15453694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:54031357..54047537hg38UCSC Ensembl
Innerchr6:53896155..53912335hg19UCSC Ensembl
Innerchr6:54004114..54020294hg18UCSC Ensembl
Innerchr6:54004114..54020294hg17UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3816181
hg1916181
hg1816181
hg1716181
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702700
Samples
Known GenesMLIP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526401
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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