A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024441



Internal ID18766973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:7902059..7930428hg38UCSC Ensembl
Innerchr8:7759581..7787950hg19UCSC Ensembl
Innerchr8:7796991..7825360hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3828370
hg1928370
hg1828370
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6981n100
Supporting Variantsnssv3753791, nssv3753792
Samples
Known GenesZNF705B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024441
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer