A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3752809



Internal ID18704404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:6450756..6552743hg38UCSC Ensembl
Innerchr7:6490387..6592374hg19UCSC Ensembl
Innerchr7:6456912..6558899hg18UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38101988
hg19101988
hg18101988
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1026878
Supporting Variants
Samples
Known GenesGRID2IP, KDELR2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3752809
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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