A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997770



Internal ID19157307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:157723830..157877526hg38UCSC Ensembl
Innerchr3:157441619..157595315hg19UCSC Ensembl
Innerchr3:158924313..159078009hg18UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg38153697
hg19153697
hg18153697
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3606386
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)nsv997770
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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