A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027345



Internal ID18769877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:5835223..5892252hg38UCSC Ensembl
Innerchr7:5874854..5931883hg19UCSC Ensembl
Innerchr7:5841380..5898409hg18UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3857030
hg1957030
hg1857030
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6242n100
Supporting Variantsnssv3752805
Samples
Known GenesOCM, ZNF815P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027345
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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