A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3177876



Internal ID22334673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:128798317..128799081hg38UCSC Ensembl
chr7:128438371..128439135hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg38765
hg19765
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8748n152
Supporting Variantsnssv14461569
SamplesHG00733
Known GenesCCDC136
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3177876
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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