A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029770



Internal ID19118989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143798851..143875061hg38UCSC Ensembl
Innerchr7:143495944..143572154hg19UCSC Ensembl
Innerchr7:143126877..143203087hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3876211
hg1976211
hg1876211
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6722n100
Supporting Variantsnssv3671146
Samples
Known GenesFAM115A, LOC154761
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029770
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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