A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017090



Internal ID19106307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:88507567..88627862hg38UCSC Ensembl
Innerchr7:88136882..88257176hg19UCSC Ensembl
Innerchr7:87974818..88095112hg18UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg38120296
hg19120295
hg18120295
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6524n100
Supporting Variantsnssv3655198
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)nsv1017090
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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