A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3759767



Internal ID19058048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:72218808..72287497hg38UCSC Ensembl
Innerchr9:74833724..74902413hg19UCSC Ensembl
Innerchr9:74023544..74092233hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3868690
hg1968690
hg1868690
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042680
Supporting Variants
Samples
Known GenesGDA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3759767
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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