A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024067



Internal ID19113284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:7177225..7202707hg38UCSC Ensembl
Innerchr5:7177338..7202820hg19UCSC Ensembl
Innerchr5:7230338..7255820hg18UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3825483
hg1925483
hg1825483
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5559n100
Supporting Variantsnssv3639623, nssv3639619, nssv3746283, nssv3746279, nssv3639620, nssv3746280, nssv3746277, nssv3746282, nssv3639624, nssv3746276, nssv3746285, nssv3639618, nssv3639621, nssv3639625, nssv3639617, nssv3746278, nssv3746284, nssv3746274, nssv3746275, nssv3639622, nssv3639626, nssv3639627, nssv3746281
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)nsv1024067
Frequency
Sample Size11257
Observed Gain0
Observed Loss23
Observed Complex0
Frequencyn/a


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