A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698522



Internal ID15435174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136497229..136498260hg38UCSC Ensembl
Innerchr8:137509472..137510503hg19UCSC Ensembl
Innerchr8:137578654..137579685hg18UCSC Ensembl
Innerchr8:137578654..137579685hg17UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg381032
hg191032
hg181032
hg171032
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522867
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698522
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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