A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034620



Internal ID18777154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:85071951..85162260hg38UCSC Ensembl
Innerchr7:84701267..84791576hg19UCSC Ensembl
Innerchr7:84539203..84629512hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3890310
hg1990310
hg1890310
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3755423
Samples
Known GenesSEMA3D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034620
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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