A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701496



Internal ID15091462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:77334838..77336864hg38UCSC Ensembl
Innerchr17:75330920..75332946hg19UCSC Ensembl
Innerchr17:72842515..72844541hg18UCSC Ensembl
Innerchr17:72842515..72844541hg17UCSC Ensembl
Cytoband17q25.2
Allele length
AssemblyAllele length
hg382027
hg192027
hg182027
hg172027
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525375
Supporting Variants
Samples
Known GenesSEPT9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701496
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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