A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3638095



Internal ID18936376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:8704114..8746922hg38UCSC Ensembl
Innerchr5:8704226..8747034hg19UCSC Ensembl
Innerchr5:8757226..8800034hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3842809
hg1942809
hg1842809
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1026017
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)nssv3638095
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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