A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515608



Internal ID15443219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:50827676..50833083hg38UCSC Ensembl
Innerchr19:51330932..51336339hg19UCSC Ensembl
Innerchr19:56022744..56028151hg18UCSC Ensembl
Innerchr19:56022744..56028151hg17UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg385408
hg195408
hg185408
hg175408
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv685909, nssv691261, nssv682845, nssv672469, nssv661493, nssv691769, nssv693312, nssv680670, nssv688635, nssv667898, nssv675409, nssv677593, nssv652533, nssv651898, nssv692297, nssv693463, nssv679799, nssv667845, nssv667445, nssv692492, nssv686448, nssv670818, nssv676551, nssv678773
Samples
Known GenesKLK15
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515608
Frequency
Sample Size2026
Observed Gain0
Observed Loss24
Observed Complex0
Frequencyn/a


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