A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17439650



Internal ID22497520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149485295..149492258hg38UCSC Ensembl
chr7:149182386..149189349hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg386964
hg196964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5926109
Supporting Variants
Samples
Known GenesZNF746
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17439650
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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