A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1125425



Internal ID19249363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:31547157..31552381hg38UCSC Ensembl
Outerchr7:31586771..31591995hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg385225
hg195225
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3961399, nssv3993534
SamplesKWS2, KWS1
Known GenesCCDC129
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1125425
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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