A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702024



Internal ID15438676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:150978271..150989138hg38UCSC Ensembl
Innerchr6:151299407..151310274hg19UCSC Ensembl
Innerchr6:151341100..151351967hg18UCSC Ensembl
Innerchr6:151391521..151402388hg17UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3810868
hg1910868
hg1810868
hg1710868
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525834
Supporting Variants
Samples
Known GenesMTHFD1L
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702024
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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