A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3757601



Internal ID19055882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:61520009..61587880hg38UCSC Ensembl
Innerchr9:44727847..44795718hg19UCSC Ensembl
Innerchr9:44667843..44735714hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3867872
hg1967872
hg1867872
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1016714
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3757601
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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