A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3565458



Internal ID18517053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:56851635..56876193hg38UCSC Ensembl
Innerchr18:54518866..54543424hg19UCSC Ensembl
Innerchr18:52669864..52694422hg18UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg3824559
hg1924559
hg1824559
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055436
Supporting Variants
Samples
Known GenesWDR7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3565458
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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