A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3730852



Internal ID19029133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:61649830..61776760hg38UCSC Ensembl
Innerchr2:61876965..62003895hg19UCSC Ensembl
Innerchr2:61730469..61857399hg18UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg38126931
hg19126931
hg18126931
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1000187
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3730852
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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