A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032876



Internal ID18775410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:70338725..70435463hg38UCSC Ensembl
Innerchr6:71048428..71145166hg19UCSC Ensembl
Innerchr6:71105149..71201887hg18UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3896739
hg1996739
hg1896739
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3658807
Samples
Known GenesFAM135A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032876
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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