A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702088



Internal ID15438740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:56691556..56691737hg38UCSC Ensembl
Innerchr19:57202924..57203105hg19UCSC Ensembl
Innerchr19:61894736..61894917hg18UCSC Ensembl
Innerchr19:61894736..61894917hg17UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38182
hg19182
hg18182
hg17182
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517449
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702088
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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