A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1075065



Internal ID18973682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:143380906..143381507hg38UCSC Ensembl
chr7:143077999..143078600hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38602
hg19602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3773025
SamplesKWP1
Known GenesZYX
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1075065
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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