A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170577



Internal ID22330832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:156760931..156761020hg38UCSC Ensembl
chr5:156187942..156188031hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14436888
SamplesHG00514
Known GenesSGCD
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3170577
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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