A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1893



Internal ID15194490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:16598310..16932548hg38UCSC Ensembl
Outerchr1:16924805..17259043hg19UCSC Ensembl
Outerchr1:16797392..17131630hg18UCSC Ensembl
Outerchr1:16670111..17004349hg17UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38334239
hg19334239
hg18334239
hg17334239
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7173
Supporting Variants
SamplesNA18555
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)nssv1893
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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