A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5314



Internal ID15196655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:16596842..16937819hg38UCSC Ensembl
Outerchr1:16923337..17264314hg19UCSC Ensembl
Outerchr1:16795924..17136901hg18UCSC Ensembl
Outerchr1:16668643..17009620hg17UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38340978
hg19340978
hg18340978
hg17340978
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7173
Supporting Variants
SamplesNA19129
Known GenesCROCC, CROCCP2, ESPNP, LOC729574, MIR3675, MST1L, MST1P2, NBPF1
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv5314
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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