A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3557524



Internal ID22426330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:73219883..73221546hg38UCSC Ensembl
chr17:71216022..71217685hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg381664
hg191664
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14281689, nssv14281688
SamplesHG00732, HG00733
Known GenesFAM104A
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3557524
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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