A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3674255



Internal ID18625850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:150474563..150525142hg38UCSC Ensembl
Innerchr7:150171651..150222230hg19UCSC Ensembl
Innerchr7:149802584..149853163hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3850580
hg1950580
hg1850580
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1031309
Supporting Variants
Samples
Known GenesGIMAP7, GIMAP8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3674255
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