A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034564



Internal ID19123786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:55537724..55565561hg38UCSC Ensembl
Innerchr7:55605417..55633254hg19UCSC Ensembl
Innerchr7:55572911..55600748hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3827838
hg1927838
hg1827838
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6361n100
Supporting Variantsnssv3661416
Samples
Known GenesVOPP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034564
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