A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv664312



Internal ID15400964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:66292519..66299570hg38UCSC Ensembl
Innerchr17:64288637..64295688hg19UCSC Ensembl
Innerchr17:61719099..61726150hg18UCSC Ensembl
Innerchr17:61719099..61726150hg17UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg387052
hg197052
hg187052
hg177052
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515667
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv664312
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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