A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4435102



Internal ID21397104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139424928..139425330hg38UCSC Ensembl
chr7:139109674..139110076hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38403
hg19403
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv775n172
Supporting Variantsnssv15747152
SamplesMDQ045
Known GenesLOC100129148
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4435102
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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