A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3586869



Internal ID18538464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:231070186..231125386hg38UCSC Ensembl
Innerchr2:231934900..231990100hg19UCSC Ensembl
Innerchr2:231643144..231698344hg18UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg3855201
hg1955201
hg1855201
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1005656
Supporting Variants
Samples
Known GenesHTR2B, PSMD1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3586869
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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