A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027869



Internal ID18770400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:89018127..89457238hg38UCSC Ensembl
Innerchr7:88647441..89086552hg19UCSC Ensembl
Innerchr7:88485377..88924488hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg38439112
hg19439112
hg18439112
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655215
Samples
Known GenesZNF804B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027869
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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