A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033932



Internal ID19123154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:150925524..150944078hg38UCSC Ensembl
Innerchr6:151246660..151265214hg19UCSC Ensembl
Innerchr6:151288353..151306907hg18UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3818555
hg1918555
hg1818555
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6162n100
Supporting Variantsnssv3654470
Samples
Known GenesMTHFD1L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033932
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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