A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696478



Internal ID15086444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:10925570..10937871hg38UCSC Ensembl
Innerchr6:10925803..10938104hg19UCSC Ensembl
Innerchr6:11033789..11046090hg18UCSC Ensembl
Innerchr6:11033789..11046090hg17UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg3812302
hg1912302
hg1812302
hg1712302
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519009
Supporting Variants
Samples
Known GenesSYCP2L
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696478
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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