A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034789



Internal ID19124010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:85508414..85545691hg38UCSC Ensembl
Innerchr7:85137730..85175007hg19UCSC Ensembl
Innerchr7:84975666..85012943hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3837278
hg1937278
hg1837278
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655172, nssv3655170, nssv3655171, nssv3755424
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)nsv1034789
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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