A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018338



Internal ID19107555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143751274..143833864hg38UCSC Ensembl
Innerchr7:143448367..143530957hg19UCSC Ensembl
Innerchr7:143079300..143161890hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3882591
hg1982591
hg1882591
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6709n100
Supporting Variantsnssv3671017
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)nsv1018338
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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