A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017891



Internal ID19107108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143751274..143816636hg38UCSC Ensembl
Innerchr7:143448367..143513729hg19UCSC Ensembl
Innerchr7:143079300..143144662hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3865363
hg1965363
hg1865363
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6709n100
Supporting Variantsnssv3670993
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)nsv1017891
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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