A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3687204



Internal ID18985485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39445895..39527663hg38UCSC Ensembl
Innerchr8:39303414..39385182hg19UCSC Ensembl
Innerchr8:39422571..39504339hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3881769
hg1981769
hg1881769
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1019950
Supporting Variants
Samples
Known GenesADAM3A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3687204
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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