A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3749542



Internal ID19047823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:136846782..136915639hg38UCSC Ensembl
Innerchr6:137167920..137236777hg19UCSC Ensembl
Innerchr6:137209613..137278470hg18UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3868858
hg1968858
hg1868858
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1025170
Supporting Variants
Samples
Known GenesPEX7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3749542
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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