A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3173112



Internal ID22332159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:130902536..130902688hg38UCSC Ensembl
chr7:130587295..130587447hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14455760
SamplesHG00733
Known GenesLOC646329
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3173112
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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