A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17442728



Internal ID22500598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:64330779..64330886hg38UCSC Ensembl
chr7:63791157..63791264hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5917436
Supporting Variants
Samples
Known GenesZNF736
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17442728
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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