A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1076957



Internal ID19325116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139424798..139425212hg38UCSC Ensembl
chr7:139109544..139109958hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38415
hg19415
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3770154
SamplesKWP1
Known GenesLOC100129148
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1076957
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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