A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv672641



Internal ID15062607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:10881942..10892266hg38UCSC Ensembl
Innerchr6:10882175..10892499hg19UCSC Ensembl
Innerchr6:10990161..11000485hg18UCSC Ensembl
Innerchr6:10990161..11000485hg17UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg3810325
hg1910325
hg1810325
hg1710325
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519302
Supporting Variants
Samples
Known GenesSYCP2L
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv672641
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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