A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021897



Internal ID18764431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:110589001..110737882hg38UCSC Ensembl
Innerchr7:110229058..110377938hg19UCSC Ensembl
Innerchr7:110016294..110165174hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38148882
hg19148881
hg18148881
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6564n100
Supporting Variantsnssv3751483
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)nsv1021897
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