A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1155849



Internal ID15507578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:43652117..43787815hg38UCSC Ensembl
Innerchr7:43691716..43827414hg19UCSC Ensembl
Innerchr7:43658241..43793939hg18UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg38135699
hg19135699
hg18135699
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv606745
Supporting Variants
Samples1780862066_A
Known GenesBLVRA, COA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1155849
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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