A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034797



Internal ID19124018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:122175201..122257055hg38UCSC Ensembl
Innerchr7:121815255..121897109hg19UCSC Ensembl
Innerchr7:121602491..121684345hg18UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg3881855
hg1981855
hg1881855
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6603n100
Supporting Variantsnssv3662120
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034797
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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