A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15750512



Internal ID21385777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139424857..139425357hg38UCSC Ensembl
chr7:139109603..139110103hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4435101
Supporting Variants
SamplesMDQ010
Known GenesLOC100129148
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15750512
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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