A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025170



Internal ID19114388
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 StatusM
Merged Variantsdgv6150n100
Supporting Variantsnssv3749542
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)nsv1025170
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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