A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032485



Internal ID19121707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:99732925..99830480hg38UCSC Ensembl
Innerchr6:100180801..100278356hg19UCSC Ensembl
Innerchr6:100287522..100385077hg18UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg3897556
hg1997556
hg1897556
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3649848
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)nsv1032485
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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