A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516441



Internal ID15443734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:8555311..8556134hg38UCSC Ensembl
Innerchr6:8555544..8556367hg19UCSC Ensembl
Innerchr6:8500543..8501366hg18UCSC Ensembl
Innerchr6:8500543..8501366hg17UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg38824
hg19824
hg18824
hg17824
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv668430, nssv691073
Samples
Known GenesLOC100506207
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516441
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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