A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1087946



Internal ID15594446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76035111..76047898hg38UCSC Ensembl
Innerchr7:75664429..75677216hg19UCSC Ensembl
Innerchr7:75502365..75515152hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3812788
hg1912788
hg1812788
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607543
Supporting Variants
Samples
Known GenesSTYXL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1087946
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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