A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697402



Internal ID15087368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:58451591..58521974hg38UCSC Ensembl
Innerchr19:58962958..59033341hg19UCSC Ensembl
Innerchr19:63654770..63725153hg18UCSC Ensembl
Innerchr19:63654770..63725153hg17UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3870384
hg1970384
hg1870384
hg1770384
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515731
Supporting Variants
Samples
Known GenesSLC27A5, ZBTB45, ZNF324, ZNF324B, ZNF446
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697402
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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