A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026738



Internal ID19115956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:94451292..94606013hg38UCSC Ensembl
Innerchr6:95161010..95315731hg19UCSC Ensembl
Innerchr6:95217731..95372452hg18UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38154722
hg19154722
hg18154722
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6096n100
Supporting Variantsnssv3751240
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)nsv1026738
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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