A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027662



Internal ID19116881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39372794..39485418hg38UCSC Ensembl
Innerchr8:39230313..39342937hg19UCSC Ensembl
Innerchr8:39349470..39462094hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38112625
hg19112625
hg18112625
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7171n100
Supporting Variantsnssv3684967
Samples
Known GenesADAM3A, ADAM5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027662
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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