A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023021



Internal ID19112238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:142717134..142851742hg38UCSC Ensembl
Innerchr8:143798552..143933158hg19UCSC Ensembl
Innerchr8:143795554..143930160hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38134609
hg19134607
hg18134607
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3757504
Samples
Known GenesGML, LOC100288181, LY6D, LYNX1, LYPD2, SLURP1, THEM6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023021
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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