A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925984



Internal ID22701211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139092583..139093859hg38UCSC Ensembl
chr7:138777329..138778605hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg381277
hg191277
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17448444
Samples
Known GenesZC3HAV1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925984
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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