A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149820



Internal ID15509057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:60072566..60627473hg38UCSC Ensembl
Innerchr18:57739798..58294706hg19UCSC Ensembl
Innerchr18:55890778..56445686hg18UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg38554908
hg19554909
hg18554909
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv577058
Supporting Variants
Samples1782681294_A
Known GenesMC4R
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149820
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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