A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1072919



Internal ID18974198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:9206570..9207071hg38UCSC Ensembl
chr2:9346699..9347200hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3764202
SamplesKWP1
Known GenesASAP2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1072919
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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