A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023376



Internal ID19112593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:111340277..111645764hg38UCSC Ensembl
Innerchr7:110980333..111285820hg19UCSC Ensembl
Innerchr7:110767569..111073056hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38305488
hg19305488
hg18305488
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6573n100
Supporting Variantsnssv3645260
Samples
Known GenesIMMP2L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023376
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