A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3576937



Internal ID18875218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:7888385..7913701hg38UCSC Ensembl
Innerchr2:8028516..8053832hg19UCSC Ensembl
Innerchr2:7945967..7971283hg18UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3825317
hg1925317
hg1825317
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1009038
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)nssv3576937
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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