A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10507



Internal ID15195605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:16600002..16934585hg38UCSC Ensembl
Outerchr1:16926497..17261080hg19UCSC Ensembl
Outerchr1:16799084..17133667hg18UCSC Ensembl
Outerchr1:16671803..17006386hg17UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38334584
hg19334584
hg18334584
hg17334584
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7173
Supporting Variants
SamplesNA18956
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)nssv10507
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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