A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1089436



Internal ID15595936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:88909179..88944157hg38UCSC Ensembl
Innerchr7:88538493..88573471hg19UCSC Ensembl
Innerchr7:88376429..88411407hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3834979
hg1934979
hg1834979
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607746
Supporting Variants
Samples
Known GenesZNF804B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1089436
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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