A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17501412



Internal ID22559350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:64322495..64324342hg38UCSC Ensembl
chr7:63782873..63784720hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg381848
hg191848
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5847093
Supporting Variants
Samples
Known GenesZNF736
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17501412
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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