A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3741549



Internal ID19039830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:155352363..155372196hg38UCSC Ensembl
Innerchr3:155070152..155089985hg19UCSC Ensembl
Innerchr3:156552846..156572679hg18UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg3819834
hg1919834
hg1819834
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1011988
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)nssv3741549
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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