A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3747237



Internal ID18698832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:69550464..71011705hg38UCSC Ensembl
Innerchr5:68846291..70307532hg19UCSC Ensembl
Innerchr5:68882047..70343288hg18UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg381461242
hg191461242
hg181461242
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1017671
Supporting Variants
Samples
Known GenesGTF2H2, GTF2H2B, GTF2H2C, GTF2H2D, GUSBP3, GUSBP9, LOC100272216, LOC441081, LOC647859, NAIP, OCLN, SERF1A, SERF1B, SMA4, SMA5, SMN1, SMN2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3747237
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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