A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3050333



Internal ID21182382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:75256021..75256021hg38UCSC Ensembl
chr7:74671598..74671598hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38908
hg19908
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14036148
SamplesNA12878
Known GenesGTF2IP1
MethodSequencing
AnalysisCombines the NGS (e.g., Illumina) and SMS (e.g., Pacbio) for detecting large and small SVs (parameters the same as commit eee31f6 of https://bitbucket.org/xianfan/hybridassemblysv)
Platform
Comments
ReferenceFan_et_al_2017
Pubmed ID28104618
Accession Number(s)nsv3050333
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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