A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419734



Internal ID21077287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:146351101..146502600hg38UCSC Ensembl
chr7:146048193..146199692hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38151500
hg19151500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155820
Samples
Known GenesCNTNAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419734
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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