A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4435231



Internal ID21397233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:16088845..16089185hg38UCSC Ensembl
chr7:16128470..16128810hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg38341
hg19341
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15750687
SamplesBTQ038
Known GenesISPD
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4435231
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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