A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028626



Internal ID19117844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:65190920..65626699hg38UCSC Ensembl
Innerchr7:64651298..65091612hg19UCSC Ensembl
Innerchr7:64288733..64729047hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38435780
hg19440315
hg18440315
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6435n100
Supporting Variantsnssv3753058
Samples
Known GenesZNF92
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028626
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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