A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023770



Internal ID19112987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:45953586..46389159hg38UCSC Ensembl
Innerchr5:45953688..46389261hg19UCSC Ensembl
Innerchr5:45989445..46425018hg18UCSC Ensembl
Cytoband5p11
Allele length
AssemblyAllele length
hg38435574
hg19435574
hg18435574
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5642n100
Supporting Variantsnssv3637893, nssv3637892
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)nsv1023770
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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