A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025246



Internal ID19114464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143747111..143849979hg38UCSC Ensembl
Innerchr7:143444204..143547072hg19UCSC Ensembl
Innerchr7:143075137..143178005hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38102869
hg19102869
hg18102869
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6710n100
Supporting Variantsnssv3670557
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)nsv1025246
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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