A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020084



Internal ID19109303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143751274..143813952hg38UCSC Ensembl
Innerchr7:143448367..143511045hg19UCSC Ensembl
Innerchr7:143079300..143141978hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3862679
hg1962679
hg1862679
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6709n100
Supporting Variantsnssv3754799
Samples
Known GenesCTAGE6, LOC154761
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020084
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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