A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026937



Internal ID19116155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:47311750..47364821hg38UCSC Ensembl
Innerchr6:47279486..47332557hg19UCSC Ensembl
Innerchr6:47387445..47440516hg18UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg3853072
hg1953072
hg1853072
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3657445
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026937
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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