A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3674697



Internal ID18972978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:155671323..155725052hg38UCSC Ensembl
Innerchr7:155464017..155517746hg19UCSC Ensembl
Innerchr7:155156778..155210507hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3853730
hg1953730
hg1853730
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1021843
Supporting Variants
Samples
Known GenesRBM33
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3674697
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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